Linked Data
MyVariant Identifiers:
chr6:g.160969559A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160548527A>T , CM000668.2:g.160548527A>T | GRCh38 |
| NC_000006.11:g.160969559A>T , CM000668.1:g.160969559A>T | GRCh37 |
| NC_000006.10:g.160889549A>T | NCBI36 |
| NG_016147.1:g.122849T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316300.10:c.5106T>A MANE Select | ENSP00000321334.6:p.Ala1702= | |
| ENST00000316300.9:c.5106T>A | ENSP00000321334.5:p.Ala1702= | |
| NM_005577.2:c.5106T>A | NP_005568.2:p.Ala1702= | |
| NM_005577.3:c.5106T>A | NP_005568.2:p.Ala1702= | |
| NM_005577.4:c.5106T>A MANE Select | NP_005568.2:p.Ala1702= |