Canonical Allele Identifier: CA1392628901
Gene:

Linked Data

dbSNP Id: rs1708402653

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743638A>G , CM000665.2:g.109743638A>G GRCh38
NC_000003.11:g.109462485A>G , CM000665.1:g.109462485A>G GRCh37
NC_000003.10:g.110945175A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63443A>G