Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19960861G>T , CM000670.2:g.19960861G>T | GRCh38 |
| NC_000008.10:g.19818372G>T , CM000670.1:g.19818372G>T | GRCh37 |
| NC_000008.9:g.19862652G>T | NCBI36 |
| NG_008855.1:g.26791G>T | |
| NG_008855.2:g.64145G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.1140-40G>T MANE Select | ENSP00000497642.1:n.1140-40G>T | |
| ENST00000650478.1:c.80-40G>T | ENSP00000497560.1:n.80-40G>T | |
| ENST00000311322.8:c.1140-40G>T | ENSP00000309757.6:n.1140-40G>T | |
| NM_000237.2:c.1140-40G>T | NP_000228.1:n.1140-40G>T | |
| NM_000237.3:c.1140-40G>T MANE Select | NP_000228.1:n.1140-40G>T |