Linked Data
MyVariant Identifiers:
chr1:g.196965213C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996083C>A , CM000663.2:g.196996083C>A | GRCh38 |
| NC_000001.10:g.196965213C>A , CM000663.1:g.196965213C>A | GRCh37 |
| NC_000001.9:g.195231836C>A | NCBI36 |
| NG_016365.1:g.23547C>A , LRG_227:g.23547C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.597C>A | ENSP00000514393.1:p.Val199= | |
| ENST00000699467.1:n.921C>A | ||
| ENST00000699468.1:c.-24-31C>A | ENSP00000514394.1:n.-24-31C>A | |
| ENST00000256785.5:c.852C>A MANE Select | ENSP00000256785.4:p.Val284= | |
| ENST00000256785.4:c.852C>A | ENSP00000256785.4:p.Val284= | |
| NM_030787.3:c.852C>A , LRG_227t1:c.852C>A | NP_110414.1:p.Val284= | |
| XM_011510020.1:c.861C>A | XP_011508322.1:p.Val287= | |
| XM_011510020.2:c.861C>A | XP_011508322.1:p.Val287= | |
| NM_030787.4:c.852C>A MANE Select | NP_110414.1:p.Val284= |