Linked Data
MyVariant Identifiers:
chr15:g.73660126T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367785T>C , CM000677.2:g.73367785T>C | GRCh38 |
| NC_000015.9:g.73660126T>C , CM000677.1:g.73660126T>C | GRCh37 |
| NC_000015.8:g.71447179T>C | NCBI36 |
| NG_009063.1:g.6480A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.486A>G MANE Select | ENSP00000261917.3:p.Ala162= | |
| ENST00000261917.3:c.486A>G | ENSP00000261917.3:p.Ala162= | |
| NM_005477.2:c.486A>G | NP_005468.1:p.Ala162= | |
| NM_005477.3:c.486A>G MANE Select | NP_005468.1:p.Ala162= |