Canonical Allele Identifier: CA562263256
Gene:

Linked Data

dbSNP Id: rs1301611665

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002815T>G , CM000667.2:g.126002815T>G GRCh38
NC_000005.9:g.125338508T>G , CM000667.1:g.125338508T>G GRCh37
NC_000005.8:g.125366407T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3525A>C
XR_948738.1:n.497+5725A>C