Canonical Allele Identifier: CA2180843916
Gene: FAM81A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419406T= , CM000677.2:g.59419406T= GRCh38
NC_000015.9:g.59711605T= , CM000677.1:g.59711605T= GRCh37
NC_000015.8:g.57498897T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17048T= ENSP00000453918.1:n.-78+17048T=
ENST00000560394.5:c.-78+17048T= ENSP00000452962.1:n.-78+17048T=
XM_006720399.1:c.-78+17048T= XP_006720462.1:n.-78+17048T=
XM_011521248.1:c.-22+17048T= XP_011519550.1:n.-22+17048T=
XM_011521248.2:c.-22+17048T= XP_011519550.1:n.-22+17048T=
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