Linked Data
MyVariant Identifiers:
chr8:g.118847773C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117835534C>A , CM000670.2:g.117835534C>A | GRCh38 |
| NC_000008.10:g.118847773C>A , CM000670.1:g.118847773C>A | GRCh37 |
| NC_000008.9:g.118916954C>A | NCBI36 |
| NG_007455.2:g.281286G>T , LRG_493:g.281286G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.541G>T | ||
| ENST00000378204.7:c.1074G>T MANE Select | ENSP00000367446.3:p.Val358= | |
| ENST00000436216.2:c.442G>T | ||
| ENST00000378204.6:c.1074G>T | ENSP00000367446.2:p.Val358= | |
| ENST00000436216.1:c.442G>T | ||
| ENST00000437196.1:c.91G>T | ENSP00000407299.1:p.Asp31Tyr | |
| NM_000127.2:c.1074G>T , LRG_493t1:c.1074G>T | NP_000118.2:p.Val358= | |
| NM_000127.3:c.1074G>T MANE Select | NP_000118.2:p.Val358= |