Canonical Allele Identifier: CA1985860006
Gene:

Linked Data

dbSNP Id: rs1857710573

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851811G>C , CM000673.2:g.80851811G>C GRCh38
NC_000011.9:g.80562854G>C , CM000673.1:g.80562854G>C GRCh37
NC_000011.8:g.80240502G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_247272.2:n.124+60480C>G