MyVariant.info:
GRCh37
chr1:g.209799264G>T
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209625919G>T , CM000663.2:g.209625919G>T | GRCh38 |
| NC_000001.10:g.209799264G>T , CM000663.1:g.209799264G>T | GRCh37 |
| NC_000001.9:g.207865887G>T | NCBI36 |
| NG_007116.1:g.31557C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356082.9:c.1705C>A MANE Select | ENSP00000348384.3:p.Arg569= | |
| ENST00000356082.8:c.1705C>A | ENSP00000348384.3:p.Arg569= | |
| ENST00000367030.7:c.1705C>A | ENSP00000355997.3:p.Arg569= | |
| ENST00000391911.5:c.1705C>A | ENSP00000375778.1:p.Arg569= | |
| NM_000228.2:c.1705C>A | NP_000219.2:p.Arg569= | |
| NM_001017402.1:c.1705C>A | NP_001017402.1:p.Arg569= | |
| NM_001127641.1:c.1705C>A | NP_001121113.1:p.Arg569= | |
| XM_005273124.3:c.1705C>A | XP_005273181.1:p.Arg569= | |
| XM_005273124.4:c.1705C>A | XP_005273181.1:p.Arg569= | |
| XM_017001272.2:c.1513C>A | XP_016856761.1:p.Arg505= | |
| NM_000228.3:c.1705C>A MANE Select | NP_000219.2:p.Arg569= | |
| NM_001017402.2:c.1705C>A | NP_001017402.1:p.Arg569= |