Canonical Allele Identifier: CA2485026941
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379668T= , CM000663.2:g.211379668T= GRCh38
NC_000001.10:g.211553010T= , CM000663.1:g.211553010T= GRCh37
NC_000001.9:g.209619633T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738446.1:n.291+2527A=