Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35851105T>G , CM000681.2:g.35851105T>G | GRCh38 |
| NC_000019.9:g.36342007T>G , CM000681.1:g.36342007T>G | GRCh37 |
| NC_000019.8:g.41033847T>G | NCBI36 |
| NG_013356.2:g.23183A>C , LRG_693:g.23183A>C | |
| NG_051206.1:g.4471T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004646.4:c.398-16A>C MANE Select | NP_004637.1:n.398-16A>C |
| ENST00000378910.10:c.398-16A>C MANE Select | ENSP00000368190.4:n.398-16A>C |
| NM_004646.3:c.398-16A>C , LRG_693t1:c.398-16A>C | NP_004637.1:n.398-16A>C |
| ENST00000353632.6:c.398-16A>C | ENSP00000343634.5:n.398-16A>C |
| ENST00000378910.9:c.398-16A>C | ENSP00000368190.4:n.398-16A>C |