Canonical Allele Identifier: CA896967325
Gene:

Linked Data

dbSNP Id: rs1460146583

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743408A>C , CM000665.2:g.109743408A>C GRCh38
NC_000003.11:g.109462255A>C , CM000665.1:g.109462255A>C GRCh37
NC_000003.10:g.110944945A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63213A>C