Canonical Allele Identifier: CA81296278
Gene:

Linked Data

dbSNP Id: rs964051395

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743556T>C , CM000665.2:g.109743556T>C GRCh38
NC_000003.11:g.109462403T>C , CM000665.1:g.109462403T>C GRCh37
NC_000003.10:g.110945093T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63361T>C