MyVariant.info:
GRCh37
chr5:g.37125432G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37125330G>T , CM000667.2:g.37125330G>T | GRCh38 |
| NC_000005.9:g.37125432G>T , CM000667.1:g.37125432G>T | GRCh37 |
| NC_000005.8:g.37161189G>T | NCBI36 |
| NG_032772.1:g.129099C>A | |
| NG_032772.2:g.129099C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000510830.2:n.1871C>A | ||
| ENST00000651892.2:c.8872C>A MANE Select | ENSP00000498265.2:p.Arg2958= | |
| ENST00000676160.1:n.733C>A | ||
| ENST00000425232.6:c.8710C>A | ENSP00000389014.2:p.Arg2904= | |
| ENST00000508244.5:c.8710C>A | ENSP00000421690.1:p.Arg2904= | |
| ENST00000509849.5:c.5884C>A | ENSP00000426337.1:n.5884C>A | |
| ENST00000509957.5:n.4053C>A | ||
| ENST00000512288.5:n.342-3546C>A | ||
| ENST00000514429.5:c.5908C>A | ENSP00000424223.1:p.Arg1970= | |
| NM_023073.3:c.8710C>A | NP_075561.3:p.Arg2904= | |
| XM_005248345.2:c.8872C>A | XP_005248402.1:p.Arg2958= | |
| XM_005248346.2:c.8869C>A | XP_005248403.1:p.Arg2957= | |
| XM_005248347.2:c.8869C>A | XP_005248404.1:p.Arg2957= | |
| XM_005248349.2:c.8761C>A | XP_005248406.1:p.Arg2921= | |
| XM_005248350.2:c.8743C>A | XP_005248407.1:p.Arg2915= | |
| XM_005248353.3:c.5515C>A | XP_005248410.1:p.Arg1839= | |
| XM_006714489.2:c.8872C>A | XP_006714552.1:p.Arg2958= | |
| XM_006714491.2:c.3445C>A | XP_006714554.1:p.Arg1149= | |
| XM_011514085.1:c.8872C>A | XP_011512387.1:p.Arg2958= | |
| XM_011514086.1:c.8872C>A | XP_011512388.1:p.Arg2958= | |
| XM_011514087.1:c.8818C>A | XP_011512389.1:p.Arg2940= | |
| XM_011514088.1:c.8764C>A | XP_011512390.1:p.Arg2922= | |
| XM_011514089.1:c.8872C>A | XP_011512391.1:p.Arg2958= | |
| XM_011514090.1:c.8554C>A | XP_011512392.1:p.Arg2852= | |
| XM_011514091.1:c.8200C>A | XP_011512393.1:p.Arg2734= | |
| XM_011514092.1:c.8872C>A | XP_011512394.1:p.Arg2958= | |
| XM_011514094.1:c.6097C>A | XP_011512396.1:p.Arg2033= | |
| XR_427661.2:n.9047C>A | ||
| XR_925644.1:n.9047C>A | ||
| XM_005248345.4:c.8872C>A | XP_005248402.1:p.Arg2958= | |
| XM_005248346.4:c.8869C>A | XP_005248403.1:p.Arg2957= | |
| XM_005248347.4:c.8869C>A | XP_005248404.1:p.Arg2957= | |
| XM_005248349.4:c.8761C>A | XP_005248406.1:p.Arg2921= | |
| XM_005248350.4:c.8743C>A | XP_005248407.1:p.Arg2915= | |
| XM_006714491.3:c.3445C>A | XP_006714554.1:p.Arg1149= | |
| XM_011514085.3:c.8872C>A | XP_011512387.1:p.Arg2958= | |
| XM_011514086.3:c.8872C>A | XP_011512388.1:p.Arg2958= | |
| XM_011514087.2:c.8818C>A | XP_011512389.1:p.Arg2940= | |
| XM_011514088.2:c.8764C>A | XP_011512390.1:p.Arg2922= | |
| XM_011514089.2:c.8872C>A | XP_011512391.1:p.Arg2958= | |
| XM_011514090.3:c.8554C>A | XP_011512392.1:p.Arg2852= | |
| XM_011514092.2:c.8872C>A | XP_011512394.1:p.Arg2958= | |
| XM_011514094.2:c.6097C>A | XP_011512396.1:p.Arg2033= | |
| XM_017009760.1:c.8683C>A | XP_016865249.1:p.Arg2895= | |
| XM_017009761.2:c.8683C>A | XP_016865250.1:p.Arg2895= | |
| XM_017009763.1:c.7879C>A | XP_016865252.1:p.Arg2627= | |
| XM_017009765.1:c.7684C>A | XP_016865254.1:p.Arg2562= | |
| XM_017009766.1:c.5515C>A | XP_016865255.1:p.Arg1839= | |
| XM_024446183.1:c.8683C>A | XP_024301951.1:p.Arg2895= | |
| XM_024446184.1:c.8554C>A | XP_024301952.1:p.Arg2852= | |
| XM_024446185.1:c.8200C>A | XP_024301953.1:p.Arg2734= | |
| XM_024446186.1:c.7879C>A | XP_024301954.1:p.Arg2627= | |
| XR_925644.2:n.9096C>A | ||
| NM_001384732.1:c.8872C>A MANE Select | NP_001371661.1:p.Arg2958= | |
| NM_023073.4:c.8710C>A | NP_075561.3:p.Arg2904= |