Linked Data
MyVariant Identifiers:
chr8:g.118849377A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837138A>T , CM000670.2:g.117837138A>T | GRCh38 |
| NC_000008.10:g.118849377A>T , CM000670.1:g.118849377A>T | GRCh37 |
| NC_000008.9:g.118918558A>T | NCBI36 |
| NG_007455.2:g.279682T>A , LRG_493:g.279682T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.493T>A | ||
| ENST00000378204.7:c.1026T>A MANE Select | ENSP00000367446.3:p.Leu342= | |
| ENST00000436216.2:c.394T>A | ||
| ENST00000378204.6:c.1026T>A | ENSP00000367446.2:p.Leu342= | |
| ENST00000436216.1:c.394T>A | ||
| ENST00000437196.1:c.74-1587T>A | ENSP00000407299.1:n.74-1587T>A | |
| NM_000127.2:c.1026T>A , LRG_493t1:c.1026T>A | NP_000118.2:p.Leu342= | |
| NM_000127.3:c.1026T>A MANE Select | NP_000118.2:p.Leu342= |