Canonical Allele Identifier: CA1889304392
Gene:

Linked Data

dbSNP Id: rs1833394874

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8659205A>G , CM000672.2:g.8659205A>G GRCh38
NC_000010.10:g.8701168A>G , CM000672.1:g.8701168A>G GRCh37
NC_000010.9:g.8741174A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.143T>C
XR_001747277.1:n.112T>C