Canonical Allele Identifier: CA2485026958
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379745A= , CM000663.2:g.211379745A= GRCh38
NC_000001.10:g.211553087A= , CM000663.1:g.211553087A= GRCh37
NC_000001.9:g.209619710A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738446.1:n.291+2450T=