Canonical Allele Identifier: CA2180855898
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs28890483

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59426970A>C , CM000677.2:g.59426970A>C GRCh38
NC_000015.9:g.59719169A>C , CM000677.1:g.59719169A>C GRCh37
NC_000015.8:g.57506461A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+24612A>C ENSP00000453918.1:n.-78+24612A>C
ENST00000560394.5:c.-78+24612A>C ENSP00000452962.1:n.-78+24612A>C
XM_006720399.1:c.-78+24612A>C XP_006720462.1:n.-78+24612A>C
XM_011521248.1:c.-22+24612A>C XP_011519550.1:n.-22+24612A>C
XM_011521248.2:c.-22+24612A>C XP_011519550.1:n.-22+24612A>C