Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21006160G>A , CM000664.2:g.21006160G>A | GRCh38 |
| NC_000002.11:g.21229032G>A , CM000664.1:g.21229032G>A | GRCh37 |
| NC_000002.10:g.21082537G>A | NCBI36 |
| NG_011793.1:g.42914C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000384.3:c.10708C>T MANE Select | NP_000375.3:p.His3570Tyr |
| ENST00000233242.5:c.10708C>T MANE Select | ENSP00000233242.1:p.His3570Tyr |
| NM_000384.2:c.10708C>T | NP_000375.2:p.His3570Tyr |
| ENST00000616098.4:c.10708C>T | ENSP00000477990.1:p.His3570Tyr |
| XM_011532809.1:c.5869+4573C>T | XP_011531111.1:n.5869+4573C>T |