Canonical Allele Identifier: CA43254727
Gene:

Linked Data

dbSNP Id: rs938215687

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458174T>C , CM000664.2:g.16458174T>C GRCh38
NC_000002.11:g.16639442T>C , CM000664.1:g.16639442T>C GRCh37
NC_000002.10:g.16502923T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3080A>G