Canonical Allele Identifier: CA2346122798
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470991T= , CM000682.2:g.2470991T= GRCh38
NC_000020.10:g.2451637T= , CM000682.1:g.2451637T= GRCh37
NC_000020.9:g.2399637T= NCBI36
NG_042057.1:g.4863A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3233A= ENSP00000456213.1:n.305-3233A=