Canonical Allele Identifier: CA1985860000
Gene:

Linked Data

dbSNP Id: rs1857710436

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851791C>G , CM000673.2:g.80851791C>G GRCh38
NC_000011.9:g.80562834C>G , CM000673.1:g.80562834C>G GRCh37
NC_000011.8:g.80240482C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_247272.2:n.124+60500G>C