Canonical Allele Identifier: CA1439212957
Gene:

Linked Data

dbSNP Id: rs1711591241

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578325C>G , CM000666.2:g.12578325C>G GRCh38
NC_000004.11:g.12579949C>G , CM000666.1:g.12579949C>G GRCh37
NC_000004.10:g.12189047C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31017G>C
XR_001741374.1:n.254+44330G>C
XR_925406.3:n.140+31017G>C