Canonical Allele Identifier: CA1267947367
Gene:

Linked Data

dbSNP Id: rs1672675779

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016187T>C , CM000664.2:g.88016187T>C GRCh38
NC_000002.11:g.88315706T>C , CM000664.1:g.88315706T>C GRCh37
NC_000002.10:g.88096821T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.532T>C
XR_940336.3:n.532T>C