Linked Data
MyVariant Identifiers:
chr8:g.118847746T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117835507T>A , CM000670.2:g.117835507T>A | GRCh38 |
| NC_000008.10:g.118847746T>A , CM000670.1:g.118847746T>A | GRCh37 |
| NC_000008.9:g.118916927T>A | NCBI36 |
| NG_007455.2:g.281313A>T , LRG_493:g.281313A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.568A>T | ||
| ENST00000378204.7:c.1101A>T MANE Select | ENSP00000367446.3:p.Pro367= | |
| ENST00000436216.2:c.469A>T | ||
| ENST00000378204.6:c.1101A>T | ENSP00000367446.2:p.Pro367= | |
| ENST00000436216.1:c.469A>T | ||
| ENST00000437196.1:c.118A>T | ENSP00000407299.1:p.Ile40Phe | |
| NM_000127.2:c.1101A>T , LRG_493t1:c.1101A>T | NP_000118.2:p.Pro367= | |
| NM_000127.3:c.1101A>T MANE Select | NP_000118.2:p.Pro367= |