Canonical Allele Identifier: CA2470007433
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8707878T= , CM000686.2:g.8707878T= GRCh38
NC_000024.9:g.8575919T= , CM000686.1:g.8575919T= GRCh37
NC_000024.8:g.8635919T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000623558.1:c.139+8846T= ENSP00000485446.1:n.139+8846T=
ENST00000624593.1:c.-57+40838A= ENSP00000485106.1:n.-57+40838A=