Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35849149T>G , CM000681.2:g.35849149T>G | GRCh38 |
| NC_000019.9:g.36340051T>G , CM000681.1:g.36340051T>G | GRCh37 |
| NC_000019.8:g.41031891T>G | NCBI36 |
| NG_013356.2:g.25139A>C , LRG_693:g.25139A>C | |
| NG_051206.1:g.2515T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004646.4:c.841-2A>C MANE Select | NP_004637.1:n.841-2A>C |
| ENST00000378910.10:c.841-2A>C MANE Select | ENSP00000368190.4:n.841-2A>C |
| NM_004646.3:c.841-2A>C , LRG_693t1:c.841-2A>C | NP_004637.1:n.841-2A>C |
| ENST00000353632.6:c.841-2A>C | ENSP00000343634.5:n.841-2A>C |
| ENST00000378910.9:c.841-2A>C | ENSP00000368190.4:n.841-2A>C |