Canonical Allele Identifier: CA2470008828
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8734282T= , CM000686.2:g.8734282T= GRCh38
NC_000024.9:g.8602323T= , CM000686.1:g.8602323T= GRCh37
NC_000024.8:g.8662323T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000623558.1:c.197-5548T= ENSP00000485446.1:n.197-5548T=
ENST00000624237.1:c.64-7773T= ENSP00000485137.1:n.64-7773T=
ENST00000624593.1:c.-57+14434A= ENSP00000485106.1:n.-57+14434A=