Canonical Allele Identifier: CA2180843970
Gene: FAM81A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419500G= , CM000677.2:g.59419500G= GRCh38
NC_000015.9:g.59711699G= , CM000677.1:g.59711699G= GRCh37
NC_000015.8:g.57498991G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17142G= ENSP00000453918.1:n.-78+17142G=
ENST00000560394.5:c.-78+17142G= ENSP00000452962.1:n.-78+17142G=
XM_006720399.1:c.-78+17142G= XP_006720462.1:n.-78+17142G=
XM_011521248.1:c.-22+17142G= XP_011519550.1:n.-22+17142G=
XM_011521248.2:c.-22+17142G= XP_011519550.1:n.-22+17142G=