Linked Data
MyVariant Identifiers:
chr8:g.118847788A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117835549A>T , CM000670.2:g.117835549A>T | GRCh38 |
| NC_000008.10:g.118847788A>T , CM000670.1:g.118847788A>T | GRCh37 |
| NC_000008.9:g.118916969A>T | NCBI36 |
| NG_007455.2:g.281271T>A , LRG_493:g.281271T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.526T>A | ||
| ENST00000378204.7:c.1059T>A MANE Select | ENSP00000367446.3:p.Ala353= | |
| ENST00000436216.2:c.427T>A | ||
| ENST00000378204.6:c.1059T>A | ENSP00000367446.2:p.Ala353= | |
| ENST00000436216.1:c.427T>A | ||
| ENST00000437196.1:c.76T>A | ENSP00000407299.1:p.Cys26Ser | |
| NM_000127.2:c.1059T>A , LRG_493t1:c.1059T>A | NP_000118.2:p.Ala353= | |
| NM_000127.3:c.1059T>A MANE Select | NP_000118.2:p.Ala353= |