Canonical Allele Identifier: CA1672973867
Gene:

Linked Data

dbSNP Id: rs1777129894

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627258A>G , CM000668.2:g.151627258A>G GRCh38
NC_000006.11:g.151948393A>G , CM000668.1:g.151948393A>G GRCh37
NC_000006.10:g.151990086A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.684A>G
XR_943115.1:n.684A>G