Canonical Allele Identifier: CA2193611489
Gene:

Linked Data

dbSNP Id: rs2082316801

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87166880A>G , CM000677.2:g.87166880A>G GRCh38
NC_000015.9:g.87710111A>G , CM000677.1:g.87710111A>G GRCh37
NC_000015.8:g.85511115A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932582.1:n.167-11347A>G
XR_932582.2:n.167-11347A>G