Canonical Allele Identifier: CA714432506
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs1425856918

Genomic Alleles

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

Transcript Alleles

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