Canonical Allele Identifier: CA2180843918
Gene: FAM81A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419411T= , CM000677.2:g.59419411T= GRCh38
NC_000015.9:g.59711610T= , CM000677.1:g.59711610T= GRCh37
NC_000015.8:g.57498902T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17053T= ENSP00000453918.1:n.-78+17053T=
ENST00000560394.5:c.-78+17053T= ENSP00000452962.1:n.-78+17053T=
XM_006720399.1:c.-78+17053T= XP_006720462.1:n.-78+17053T=
XM_011521248.1:c.-22+17053T= XP_011519550.1:n.-22+17053T=
XM_011521248.2:c.-22+17053T= XP_011519550.1:n.-22+17053T=