Canonical Allele Identifier: CA271499813
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs372156772

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419497C>A , CM000677.2:g.59419497C>A GRCh38
NC_000015.9:g.59711696C>A , CM000677.1:g.59711696C>A GRCh37
NC_000015.8:g.57498988C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17139C>A ENSP00000453918.1:n.-78+17139C>A
ENST00000560394.5:c.-78+17139C>A ENSP00000452962.1:n.-78+17139C>A
XM_006720399.1:c.-78+17139C>A XP_006720462.1:n.-78+17139C>A
XM_011521248.1:c.-22+17139C>A XP_011519550.1:n.-22+17139C>A
XM_011521248.2:c.-22+17139C>A XP_011519550.1:n.-22+17139C>A