Canonical Allele Identifier: CA127232026
Gene:

Linked Data

dbSNP Id: rs546244126

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002813C>G , CM000667.2:g.126002813C>G GRCh38
NC_000005.9:g.125338506C>G , CM000667.1:g.125338506C>G GRCh37
NC_000005.8:g.125366405C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3527G>C
XR_948738.1:n.497+5727G>C