Canonical Allele Identifier: CA2485026929
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379635C= , CM000663.2:g.211379635C= GRCh38
NC_000001.10:g.211552977C= , CM000663.1:g.211552977C= GRCh37
NC_000001.9:g.209619600C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738446.1:n.292-2519G=