Canonical Allele Identifier: CA764892147
Gene:

Linked Data

dbSNP Id: rs1164154966

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216596T>C , CM000664.2:g.218216596T>C GRCh38
NC_000002.11:g.219081319T>C , CM000664.1:g.219081319T>C GRCh37
NC_000002.10:g.218789564T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.349A>G
XR_923908.1:n.346A>G