Canonical Allele Identifier: CA1392628877
Gene:

Linked Data

dbSNP Id: rs1708402433

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743585A>G , CM000665.2:g.109743585A>G GRCh38
NC_000003.11:g.109462432A>G , CM000665.1:g.109462432A>G GRCh37
NC_000003.10:g.110945122A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63390A>G