Canonical Allele Identifier: CA562115671
Gene:

Linked Data

dbSNP Id: rs1279061990

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660952G>C , CM000667.2:g.113660952G>C GRCh38
NC_000005.9:g.112996649G>C , CM000667.1:g.112996649G>C GRCh37
NC_000005.8:g.113024548G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27588G>C