Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74693640T>A , CM000667.2:g.74693640T>A | GRCh38 |
| NC_000005.9:g.73989465T>A , CM000667.1:g.73989465T>A | GRCh37 |
| NC_000005.8:g.74025221T>A | NCBI36 |
| NG_009770.1:g.13497T>A | |
| NG_009770.2:g.58618T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000521.4:c.447T>A MANE Select | NP_000512.2:p.Tyr149Ter |
| ENST00000261416.12:c.447T>A MANE Select | ENSP00000261416.7:p.Tyr149Ter |
| NM_000521.3:c.447T>A | NP_000512.1:p.Tyr149Ter |
| NM_001292004.1:c.-229T>A | NP_001278933.1:n.-229T>A |
| NM_001292004.2:c.-229T>A | NP_001278933.1:n.-229T>A |
| ENST00000261416.11:c.447T>A | ENSP00000261416.7:p.Tyr149Ter |
| ENST00000510820.1:n.166T>A | |
| ENST00000511181.5:c.-229T>A | ENSP00000426285.1:n.-229T>A |
| ENST00000513079.5:n.512T>A |