Canonical Allele Identifier: CA669472896
Gene:

Linked Data

dbSNP Id: rs1410226108

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697607T>C , CM000672.2:g.8697607T>C GRCh38
NC_000010.10:g.8739570T>C , CM000672.1:g.8739570T>C GRCh37
NC_000010.9:g.8779576T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27806A>G