Canonical Allele Identifier: CA1769514531
Gene:

Linked Data

dbSNP Id: rs1563254716

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734919G>C , CM000670.2:g.20734919G>C GRCh38
NC_000008.10:g.20592430G>C , CM000670.1:g.20592430G>C GRCh37
NC_000008.9:g.20636710G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55527G>C