Canonical Allele Identifier: CA2346122791
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470982G= , CM000682.2:g.2470982G= GRCh38
NC_000020.10:g.2451628G= , CM000682.1:g.2451628G= GRCh37
NC_000020.9:g.2399628G= NCBI36
NG_042057.1:g.4872C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3224C= ENSP00000456213.1:n.305-3224C=