Canonical Allele Identifier: CA271499818
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs185860414

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419513C>T , CM000677.2:g.59419513C>T GRCh38
NC_000015.9:g.59711712C>T , CM000677.1:g.59711712C>T GRCh37
NC_000015.8:g.57499004C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17155C>T ENSP00000453918.1:n.-78+17155C>T
ENST00000560394.5:c.-78+17155C>T ENSP00000452962.1:n.-78+17155C>T
XM_006720399.1:c.-78+17155C>T XP_006720462.1:n.-78+17155C>T
XM_011521248.1:c.-22+17155C>T XP_011519550.1:n.-22+17155C>T
XM_011521248.2:c.-22+17155C>T XP_011519550.1:n.-22+17155C>T