Canonical Allele Identifier: CA1580179069
Gene:

Linked Data

dbSNP Id: rs1749025289

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002814T>C , CM000667.2:g.126002814T>C GRCh38
NC_000005.9:g.125338507T>C , CM000667.1:g.125338507T>C GRCh37
NC_000005.8:g.125366406T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3526A>G
XR_948738.1:n.497+5726A>G