Canonical Allele Identifier: CA127231915
Gene:

Linked Data

dbSNP Id: rs967703759

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002683C>T , CM000667.2:g.126002683C>T GRCh38
NC_000005.9:g.125338376C>T , CM000667.1:g.125338376C>T GRCh37
NC_000005.8:g.125366275C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3657G>A
XR_948738.1:n.497+5857G>A