Canonical Allele Identifier: CA1267947229
Gene:

Linked Data

dbSNP Id: rs1438186247

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016035G>C , CM000664.2:g.88016035G>C GRCh38
NC_000002.11:g.88315554G>C , CM000664.1:g.88315554G>C GRCh37
NC_000002.10:g.88096669G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.380G>C
XR_940336.3:n.380G>C