Canonical Allele Identifier: CA2470007435
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8707896C= , CM000686.2:g.8707896C= GRCh38
NC_000024.9:g.8575937C= , CM000686.1:g.8575937C= GRCh37
NC_000024.8:g.8635937C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000623558.1:c.139+8864C= ENSP00000485446.1:n.139+8864C=
ENST00000624593.1:c.-57+40820G= ENSP00000485106.1:n.-57+40820G=