Canonical Allele Identifier: CA2470005034
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8665694G= , CM000686.2:g.8665694G= GRCh38
NC_000024.9:g.8533735G= , CM000686.1:g.8533735G= GRCh37
NC_000024.8:g.8593735G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.-56-7004C= ENSP00000485106.1:n.-56-7004C=