Canonical Allele Identifier: CA1672973882
Gene:

Linked Data

dbSNP Id: rs1777130517

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627289C>A , CM000668.2:g.151627289C>A GRCh38
NC_000006.11:g.151948424C>A , CM000668.1:g.151948424C>A GRCh37
NC_000006.10:g.151990117C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.715C>A
XR_943115.1:n.715C>A