MyVariant.info:
GRCh37
chr7:g.95813688G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.96184376G>T , CM000669.2:g.96184376G>T | GRCh38 |
| NC_000007.13:g.95813688G>T , CM000669.1:g.95813688G>T | GRCh37 |
| NC_000007.12:g.95651624G>T | NCBI36 |
| NG_012247.1:g.142772C>A | |
| NG_012247.2:g.142772C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265631.10:c.1078C>A MANE Select | ENSP00000265631.6:p.Arg360= | |
| ENST00000265631.9:c.1078C>A | ENSP00000265631.5:p.Arg360= | |
| ENST00000416240.6:c.1081C>A | ENSP00000400101.2:p.Arg361= | |
| ENST00000484495.5:n.231C>A | ||
| ENST00000490072.5:n.145C>A | ||
| ENST00000492869.1:n.199C>A | ||
| NM_001160210.1:c.1081C>A | NP_001153682.1:p.Arg361= | |
| NM_014251.2:c.1078C>A | NP_055066.1:p.Arg360= | |
| NR_027662.1:n.1153C>A | ||
| XM_006715831.2:c.1111C>A | XP_006715894.1:p.Arg371= | |
| XM_011515727.1:c.1111C>A | XP_011514029.1:p.Arg371= | |
| XM_011515728.1:c.226C>A | XP_011514030.1:p.Arg76= | |
| XM_006715831.4:c.1111C>A | XP_006715894.1:p.Arg371= | |
| XM_011515727.3:c.1111C>A | XP_011514029.1:p.Arg371= | |
| XM_017011663.1:c.1069C>A | XP_016867152.1:p.Arg357= | |
| XM_017011664.2:c.226C>A | XP_016867153.1:p.Arg76= | |
| XM_017011665.1:c.226C>A | XP_016867154.1:p.Arg76= | |
| XR_001744525.2:n.1249C>A | ||
| XR_002956405.1:n.1882C>A | ||
| NM_014251.3:c.1078C>A MANE Select | NP_055066.1:p.Arg360= | |
| NR_027662.2:n.1104C>A | ||
| NM_001160210.2:c.1081C>A | NP_001153682.1:p.Arg361= |