Canonical Allele Identifier: CA1889344495
Gene:

Linked Data

dbSNP Id: rs1832129895

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697521C>G , CM000672.2:g.8697521C>G GRCh38
NC_000010.10:g.8739484C>G , CM000672.1:g.8739484C>G GRCh37
NC_000010.9:g.8779490C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27720G>C