Canonical Allele Identifier: CA207989732
Gene:

Linked Data

dbSNP Id: rs969997812

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812896A>G , CM000672.2:g.57812896A>G GRCh38
NC_000010.10:g.59572656A>G , CM000672.1:g.59572656A>G GRCh37
NC_000010.9:g.59242662A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34396T>C
XR_001747454.1:n.85+34396T>C