Canonical Allele Identifier: CA2485026939
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379666T= , CM000663.2:g.211379666T= GRCh38
NC_000001.10:g.211553008T= , CM000663.1:g.211553008T= GRCh37
NC_000001.9:g.209619631T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738446.1:n.291+2529A=