Linked Data
ClinVar Variation Id:
2747530
ClinVar RCV Id:
RCV003497765
MyVariant Identifiers:
chr8:g.118849434A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837195A>G , CM000670.2:g.117837195A>G | GRCh38 |
| NC_000008.10:g.118849434A>G , CM000670.1:g.118849434A>G | GRCh37 |
| NC_000008.9:g.118918615A>G | NCBI36 |
| NG_007455.2:g.279625T>C , LRG_493:g.279625T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.436T>C | ||
| ENST00000378204.7:c.969T>C MANE Select | ENSP00000367446.3:p.Asp323= | |
| ENST00000436216.2:c.337T>C | ||
| ENST00000378204.6:c.969T>C | ENSP00000367446.2:p.Asp323= | |
| ENST00000436216.1:c.337T>C | ||
| ENST00000437196.1:c.74-1644T>C | ENSP00000407299.1:n.74-1644T>C | |
| NM_000127.2:c.969T>C , LRG_493t1:c.969T>C | NP_000118.2:p.Asp323= | |
| NM_000127.3:c.969T>C MANE Select | NP_000118.2:p.Asp323= |