Canonical Allele Identifier: CA665341663
Gene:

Linked Data

dbSNP Id: rs1380507501

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318680C>G , CM000672.2:g.43318680C>G GRCh38
NC_000010.10:g.43814128C>G , CM000672.1:g.43814128C>G GRCh37
NC_000010.9:g.43134134C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+85C>G
XR_945902.2:n.198+85C>G