Canonical Allele Identifier: CA788849927
Gene:

Linked Data

dbSNP Id: rs1382626556

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748274A>G , CM000666.2:g.148748274A>G GRCh38
NC_000004.11:g.149669426A>G , CM000666.1:g.149669426A>G GRCh37
NC_000004.10:g.149888876A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118483A>G