Canonical Allele Identifier: CA1267947277
Gene:

Linked Data

dbSNP Id: rs1672672900

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016093C>A , CM000664.2:g.88016093C>A GRCh38
NC_000002.11:g.88315612C>A , CM000664.1:g.88315612C>A GRCh37
NC_000002.10:g.88096727C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.438C>A
XR_940336.3:n.438C>A