Canonical Allele Identifier: CA2815053035
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470972T>A , CM000682.2:g.2470972T>A GRCh38
NC_000020.10:g.2451618T>A , CM000682.1:g.2451618T>A GRCh37
NC_000020.9:g.2399618T>A NCBI36
NG_042057.1:g.4882A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3214A>T ENSP00000456213.1:n.305-3214A>T