Canonical Allele Identifier: CA1267947344
Gene:

Linked Data

dbSNP Id: rs910474490

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016162A>C , CM000664.2:g.88016162A>C GRCh38
NC_000002.11:g.88315681A>C , CM000664.1:g.88315681A>C GRCh37
NC_000002.10:g.88096796A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.507A>C
XR_940336.3:n.507A>C