Canonical Allele Identifier: CA14948770
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23891811G>A , CM000684.2:g.23891811G>A GRCh38
NC_000022.10:g.24233998G>A , CM000684.1:g.24233998G>A GRCh37
NC_000022.9:g.22563998G>A NCBI36
NG_012099.1:g.2434G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000433835.3:c.432-2961G>A ENSP00000400325.3:n.432-2961G>A