Canonical Allele Identifier: CA970390884
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs2081161599

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419539C>G , CM000677.2:g.59419539C>G GRCh38
NC_000015.9:g.59711738C>G , CM000677.1:g.59711738C>G GRCh37
NC_000015.8:g.57499030C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17181C>G ENSP00000453918.1:n.-78+17181C>G
ENST00000560394.5:c.-78+17181C>G ENSP00000452962.1:n.-78+17181C>G
XM_006720399.1:c.-78+17181C>G XP_006720462.1:n.-78+17181C>G
XM_011521248.1:c.-22+17181C>G XP_011519550.1:n.-22+17181C>G
XM_011521248.2:c.-22+17181C>G XP_011519550.1:n.-22+17181C>G