MyVariant.info:
GRCh37
chr10:g.79551640C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.77791882C>A , CM000672.2:g.77791882C>A | GRCh38 |
| NC_000010.10:g.79551640C>A , CM000672.1:g.79551640C>A | GRCh37 |
| NC_000010.9:g.79221646C>A | NCBI36 |
| NG_011484.1:g.139709G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372391.7:c.*558G>T MANE Select | ENSP00000361467.2:n.*558G>T | |
| ENST00000372391.6:c.*558G>T | ENSP00000361467.2:n.*558G>T | |
| ENST00000424842.5:c.3201G>T | ENSP00000394797.1:n.3201G>T | |
| ENST00000475613.6:n.6155G>T | ||
| NM_004747.3:c.*558G>T | NP_004738.3:n.*558G>T | |
| XM_005270276.3:c.*558G>T | XP_005270333.1:n.*558G>T | |
| XM_006718056.2:c.*558G>T | XP_006718119.1:n.*558G>T | |
| XM_011540341.1:c.*558G>T | XP_011538643.1:n.*558G>T | |
| XM_011540342.1:c.*558G>T | XP_011538644.1:n.*558G>T | |
| XM_011540343.1:c.*558G>T | XP_011538645.1:n.*558G>T | |
| XM_011540344.1:c.*558G>T | XP_011538646.1:n.*558G>T | |
| XM_011540345.1:c.*558G>T | XP_011538647.1:n.*558G>T | |
| XM_011540347.1:c.*558G>T | XP_011538649.1:n.*558G>T | |
| XM_005270276.4:c.*558G>T | XP_005270333.1:n.*558G>T | |
| XM_006718056.3:c.*558G>T | XP_006718119.1:n.*558G>T | |
| XM_011540341.3:c.*558G>T | XP_011538643.1:n.*558G>T | |
| XM_011540344.2:c.*558G>T | XP_011538646.1:n.*558G>T | |
| XM_011540347.2:c.*558G>T | XP_011538649.1:n.*558G>T | |
| XM_017016913.1:c.*558G>T | XP_016872402.1:n.*558G>T | |
| XM_017016914.1:c.*558G>T | XP_016872403.1:n.*558G>T | |
| XM_017016915.1:c.*558G>T | XP_016872404.1:n.*558G>T | |
| XM_024448250.1:c.*558G>T | XP_024304018.1:n.*558G>T | |
| NM_004747.4:c.*558G>T MANE Select | NP_004738.3:n.*558G>T |