Linked Data
MyVariant Identifiers:
chr1:g.169454942C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169485704C>A , CM000663.2:g.169485704C>A | GRCh38 |
| NC_000001.10:g.169454942C>A , CM000663.1:g.169454942C>A | GRCh37 |
| NC_000001.9:g.167721566C>A | NCBI36 |
| NG_008255.1:g.5267G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236137.10:c.63G>T MANE Select | ENSP00000236137.5:p.Arg21= | |
| ENST00000646596.1:c.63G>T | ENSP00000494404.1:p.Arg21= | |
| ENST00000236137.9:c.63G>T | ENSP00000236137.5:p.Arg21= | |
| ENST00000367804.4:c.63G>T | ENSP00000356778.3:p.Arg21= | |
| NM_006996.2:c.63G>T | NP_008927.1:p.Arg21= | |
| XM_011509076.1:c.12+349G>T | XP_011507378.1:n.12+349G>T | |
| XM_011509077.1:c.63G>T | XP_011507379.1:p.Arg21= | |
| NM_001319667.1:c.63G>T | NP_001306596.1:p.Arg21= | |
| NM_006996.3:c.63G>T MANE Select | NP_008927.1:p.Arg21= |