Canonical Allele Identifier: CA1042430017
Gene:

Linked Data

dbSNP Id: rs1689246471

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216579A>G , CM000664.2:g.218216579A>G GRCh38
NC_000002.11:g.219081302A>G , CM000664.1:g.219081302A>G GRCh37
NC_000002.10:g.218789547A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.366T>C
XR_923908.1:n.363T>C