Canonical Allele Identifier: CA125569073
Gene:

Linked Data

dbSNP Id: rs919546794

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660887G>T , CM000667.2:g.113660887G>T GRCh38
NC_000005.9:g.112996584G>T , CM000667.1:g.112996584G>T GRCh37
NC_000005.8:g.113024483G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27523G>T