Canonical Allele Identifier: CA1769199554
Gene:

Linked Data

dbSNP Id: rs1563697599

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130208G>C , CM000670.2:g.20130208G>C GRCh38
NC_000008.10:g.19987719G>C , CM000670.1:g.19987719G>C GRCh37
NC_000008.9:g.20031999G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949563.1:n.3408+289G>C
XR_949563.2:n.3400+289G>C