Canonical Allele Identifier: CA803406359
Gene:

Linked Data

dbSNP Id: rs1236452314

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002727T>C , CM000667.2:g.126002727T>C GRCh38
NC_000005.9:g.125338420T>C , CM000667.1:g.125338420T>C GRCh37
NC_000005.8:g.125366319T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3613A>G
XR_948738.1:n.497+5813A>G