Linked Data
MyVariant Identifiers:
chr1:g.196965177A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996047A>T , CM000663.2:g.196996047A>T | GRCh38 |
| NC_000001.10:g.196965177A>T , CM000663.1:g.196965177A>T | GRCh37 |
| NC_000001.9:g.195231800A>T | NCBI36 |
| NG_016365.1:g.23511A>T , LRG_227:g.23511A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.561A>T | ENSP00000514393.1:p.Ile187= | |
| ENST00000699467.1:n.885A>T | ||
| ENST00000699468.1:c.-24-67A>T | ENSP00000514394.1:n.-24-67A>T | |
| ENST00000256785.5:c.816A>T MANE Select | ENSP00000256785.4:p.Ile272= | |
| ENST00000256785.4:c.816A>T | ENSP00000256785.4:p.Ile272= | |
| NM_030787.3:c.816A>T , LRG_227t1:c.816A>T | NP_110414.1:p.Ile272= | |
| XM_011510020.1:c.825A>T | XP_011508322.1:p.Ile275= | |
| XM_011510020.2:c.825A>T | XP_011508322.1:p.Ile275= | |
| NM_030787.4:c.816A>T MANE Select | NP_110414.1:p.Ile272= |