Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240878076A>T , CM000664.2:g.240878076A>T | GRCh38 |
| NC_000002.11:g.241817493A>T , CM000664.1:g.241817493A>T | GRCh37 |
| NC_000002.10:g.241466166A>T | NCBI36 |
| NG_008005.1:g.14332A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000030.3:c.997A>T MANE Select | NP_000021.1:p.Arg333Ter |
| ENST00000307503.4:c.997A>T MANE Select | ENSP00000302620.3:p.Arg333Ter |
| NM_000030.2:c.997A>T | NP_000021.1:p.Arg333Ter |
| ENST00000307503.3:c.997A>T | ENSP00000302620.3:p.Arg333Ter |
| ENST00000470255.1:n.775A>T |