Canonical Allele Identifier: CA539586556
Gene:

Linked Data

dbSNP Id: rs1455658601

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216584T>C , CM000664.2:g.218216584T>C GRCh38
NC_000002.11:g.219081307T>C , CM000664.1:g.219081307T>C GRCh37
NC_000002.10:g.218789552T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.361A>G
XR_923908.1:n.358A>G