Linked Data
MyVariant Identifiers:
chr1:g.196965159G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996029G>T , CM000663.2:g.196996029G>T | GRCh38 |
| NC_000001.10:g.196965159G>T , CM000663.1:g.196965159G>T | GRCh37 |
| NC_000001.9:g.195231782G>T | NCBI36 |
| NG_016365.1:g.23493G>T , LRG_227:g.23493G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.543G>T | ENSP00000514393.1:p.Val181= | |
| ENST00000699467.1:n.867G>T | ||
| ENST00000699468.1:c.-24-85G>T | ENSP00000514394.1:n.-24-85G>T | |
| ENST00000256785.5:c.798G>T MANE Select | ENSP00000256785.4:p.Val266= | |
| ENST00000256785.4:c.798G>T | ENSP00000256785.4:p.Val266= | |
| NM_030787.3:c.798G>T , LRG_227t1:c.798G>T | NP_110414.1:p.Val266= | |
| XM_011510020.1:c.807G>T | XP_011508322.1:p.Val269= | |
| XM_011510020.2:c.807G>T | XP_011508322.1:p.Val269= | |
| NM_030787.4:c.798G>T MANE Select | NP_110414.1:p.Val266= |