Canonical Allele Identifier: CA2602998746
Gene:

Linked Data

dbSNP Id: rs2107331635

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743570G>A , CM000665.2:g.109743570G>A GRCh38
NC_000003.11:g.109462417G>A , CM000665.1:g.109462417G>A GRCh37
NC_000003.10:g.110945107G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63375G>A