Canonical Allele Identifier: CA1898741275
Gene:

Linked Data

dbSNP Id: rs4747639

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075711A>C , CM000672.2:g.29075711A>C GRCh38
NC_000010.10:g.29364640A>C , CM000672.1:g.29364640A>C GRCh37
NC_000010.9:g.29404646A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001747284.1:n.127-3781A>C