Canonical Allele Identifier: CA2541504982
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.14926109A>G , CM000664.2:g.14926109A>G GRCh38
NC_000002.11:g.15066233A>G , CM000664.1:g.15066233A>G GRCh37
NC_000002.10:g.14983684A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922818.1:n.205-146962T>C