dbSNP:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.172447373A>C , CM000665.2:g.172447373A>C | GRCh38 |
| NC_000003.11:g.172165163A>C , CM000665.1:g.172165163A>C | GRCh37 |
| NC_000003.10:g.173647857A>C | NCBI36 |
| NG_021159.1:g.6084T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000241256.3:c.796+245T>G MANE Select | ENSP00000241256.2:n.796+245T>G | |
| ENST00000241256.2:c.796+245T>G | ENSP00000241256.2:n.796+245T>G | |
| NM_198407.2:c.796+245T>G MANE Select | NP_940799.1:n.796+245T>G |