Linked Data
MyVariant Identifiers:
chr8:g.118849419C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837180C>A , CM000670.2:g.117837180C>A | GRCh38 |
| NC_000008.10:g.118849419C>A , CM000670.1:g.118849419C>A | GRCh37 |
| NC_000008.9:g.118918600C>A | NCBI36 |
| NG_007455.2:g.279640G>T , LRG_493:g.279640G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.451G>T | ||
| ENST00000378204.7:c.984G>T MANE Select | ENSP00000367446.3:p.Leu328= | |
| ENST00000436216.2:c.352G>T | ||
| ENST00000378204.6:c.984G>T | ENSP00000367446.2:p.Leu328= | |
| ENST00000436216.1:c.352G>T | ||
| ENST00000437196.1:c.74-1629G>T | ENSP00000407299.1:n.74-1629G>T | |
| NM_000127.2:c.984G>T , LRG_493t1:c.984G>T | NP_000118.2:p.Leu328= | |
| NM_000127.3:c.984G>T MANE Select | NP_000118.2:p.Leu328= |