Canonical Allele Identifier: CA2199721330
Gene:

Linked Data

dbSNP Id: rs2059765569

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99817253A>G , CM000677.2:g.99817253A>G GRCh38
NC_000015.9:g.100357458A>G , CM000677.1:g.100357458A>G GRCh37
NC_000015.8:g.98174981A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932717.1:n.408+4167A>G
XR_932718.1:n.408+4167A>G
XR_932719.1:n.514+8951A>G
XR_932720.1:n.409-1685A>G
NR_135737.1:n.346+4167A>G