Canonical Allele Identifier: CA1580179094
Gene:

Linked Data

dbSNP Id: rs1749025957

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002875G>C , CM000667.2:g.126002875G>C GRCh38
NC_000005.9:g.125338568G>C , CM000667.1:g.125338568G>C GRCh37
NC_000005.8:g.125366467G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948737.1:n.565+3465C>G
XR_948738.1:n.497+5665C>G