MyVariant.info:
GRCh38
chr6:g.31633043A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31633043A>T , CM000668.2:g.31633043A>T | GRCh38 |
| NC_000006.11:g.31600820A>T , CM000668.1:g.31600820A>T | GRCh37 |
| NC_000006.10:g.31708799A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376033.3:c.4319+51A>T MANE Select | ENSP00000365201.2:n.4319+51A>T | |
| ENST00000376007.8:c.4319+51A>T | ENSP00000365175.4:n.4319+51A>T | |
| ENST00000376033.2:c.4319+51A>T | ENSP00000365201.2:n.4319+51A>T | |
| NM_004638.3:c.4319+51A>T | NP_004629.3:n.4319+51A>T | |
| NM_080686.2:c.4319+51A>T | NP_542417.2:n.4319+51A>T | |
| XM_011514890.1:c.4319+51A>T | XP_011513192.1:n.4319+51A>T | |
| XM_017011274.1:c.4319+51A>T | XP_016866763.1:n.4319+51A>T | |
| NM_004638.4:c.4319+51A>T MANE Select | NP_004629.3:n.4319+51A>T | |
| NM_080686.3:c.4319+51A>T | NP_542417.2:n.4319+51A>T |