dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19966981T>A , CM000670.2:g.19966981T>A | GRCh38 |
| NC_000008.10:g.19824492T>A , CM000670.1:g.19824492T>A | GRCh37 |
| NC_000008.9:g.19868772T>A | NCBI36 |
| NG_008855.1:g.32911T>A | |
| NG_008855.2:g.70265T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.*1671T>A MANE Select | ENSP00000497642.1:n.*1671T>A | |
| ENST00000650478.1:c.2039T>A | ENSP00000497560.1:n.2039T>A | |
| ENST00000311322.8:c.*1671T>A | ENSP00000309757.6:n.*1671T>A | |
| NM_000237.2:c.*1671T>A | NP_000228.1:n.*1671T>A | |
| NM_000237.3:c.*1671T>A MANE Select | NP_000228.1:n.*1671T>A |