Linked Data
MyVariant Identifiers:
chr1:g.196965156A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996026A>G , CM000663.2:g.196996026A>G | GRCh38 |
| NC_000001.10:g.196965156A>G , CM000663.1:g.196965156A>G | GRCh37 |
| NC_000001.9:g.195231779A>G | NCBI36 |
| NG_016365.1:g.23490A>G , LRG_227:g.23490A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.540A>G | ENSP00000514393.1:p.Gln180= | |
| ENST00000699467.1:n.864A>G | ||
| ENST00000699468.1:c.-24-88A>G | ENSP00000514394.1:n.-24-88A>G | |
| ENST00000256785.5:c.795A>G MANE Select | ENSP00000256785.4:p.Gln265= | |
| ENST00000256785.4:c.795A>G | ENSP00000256785.4:p.Gln265= | |
| NM_030787.3:c.795A>G , LRG_227t1:c.795A>G | NP_110414.1:p.Gln265= | |
| XM_011510020.1:c.804A>G | XP_011508322.1:p.Gln268= | |
| XM_011510020.2:c.804A>G | XP_011508322.1:p.Gln268= | |
| NM_030787.4:c.795A>G MANE Select | NP_110414.1:p.Gln265= |