MyVariant.info:
GRCh37
chr5:g.37045621T>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37045519T>A , CM000667.2:g.37045519T>A | GRCh38 |
| NC_000005.9:g.37045621T>A , CM000667.1:g.37045621T>A | GRCh37 |
| NC_000005.8:g.37081378T>A | NCBI36 |
| NG_006987.1:g.173637T>A | |
| NG_006987.2:g.173637T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.6420T>A MANE Select | ENSP00000282516.8:p.Leu2140= | |
| ENST00000652901.1:c.6420T>A | ENSP00000499536.1:p.Leu2140= | |
| ENST00000282516.12:c.6420T>A | ENSP00000282516.8:p.Leu2140= | |
| ENST00000448238.2:c.6420T>A | ENSP00000406266.2:p.Leu2140= | |
| ENST00000621733.1:c.1-19059T>A | ENSP00000480694.1:n.1-19059T>A | |
| NM_015384.4:c.6420T>A | NP_056199.2:p.Leu2140= | |
| NM_133433.3:c.6420T>A | NP_597677.2:p.Leu2140= | |
| XM_005248280.2:c.6420T>A | XP_005248337.1:p.Leu2140= | |
| XM_005248282.3:c.5676T>A | XP_005248339.2:p.Leu1892= | |
| XM_006714467.2:c.6420T>A | XP_006714530.1:p.Leu2140= | |
| XM_006714468.1:c.6222T>A | XP_006714531.1:p.Leu2074= | |
| XM_011514014.1:c.6039T>A | XP_011512316.1:p.Leu2013= | |
| XM_011514015.1:c.6420T>A | XP_011512317.1:p.Leu2140= | |
| XM_005248280.3:c.6420T>A | XP_005248337.1:p.Leu2140= | |
| XM_005248282.5:c.5760T>A | XP_005248339.3:p.Leu1920= | |
| XM_006714468.2:c.6222T>A | XP_006714531.1:p.Leu2074= | |
| XM_017009329.1:c.6420T>A | XP_016864818.1:p.Leu2140= | |
| XM_017009330.2:c.4803T>A | XP_016864819.1:p.Leu1601= | |
| XM_017009331.1:c.4794T>A | XP_016864820.1:p.Leu1598= | |
| NM_133433.4:c.6420T>A MANE Select | NP_597677.2:p.Leu2140= | |
| NM_015384.5:c.6420T>A | NP_056199.2:p.Leu2140= |