Canonical Allele Identifier: CA764892121
Gene:

Linked Data

dbSNP Id: rs1328261986

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216580T>G , CM000664.2:g.218216580T>G GRCh38
NC_000002.11:g.219081303T>G , CM000664.1:g.219081303T>G GRCh37
NC_000002.10:g.218789548T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.365A>C
XR_923908.1:n.362A>C