Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47836260C>T , CM000681.2:g.47836260C>T | GRCh38 |
| NC_000019.9:g.48339517C>T , CM000681.1:g.48339517C>T | GRCh37 |
| NC_000019.8:g.53031329C>T | NCBI36 |
| NG_008605.1:g.19419C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000554.6:c.118C>T MANE Select | NP_000545.1:p.Arg40Trp |
| ENST00000221996.12:c.118C>T MANE Select | ENSP00000221996.5:p.Arg40Trp |
| NM_000554.4:c.118C>T | NP_000545.1:p.Arg40Trp |
| NM_000554.5:c.118C>T | NP_000545.1:p.Arg40Trp |
| ENST00000221996.11:c.118C>T | ENSP00000221996.5:p.Arg40Trp |
| ENST00000539067.5:c.118C>T | ENSP00000445565.1:p.Arg40Trp |
| ENST00000556527.1:n.95C>T | |
| ENST00000566686.5:c.118C>T | ENSP00000457808.2:p.Arg40Trp |
| ENST00000613299.1:c.100+1717C>T | ENSP00000478106.1:n.100+1717C>T |