Canonical Allele Identifier: CA177899574
Gene: FAM110B HGNC NCBI

Linked Data

dbSNP Id: rs13273891

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58073900G>A , CM000670.2:g.58073900G>A GRCh38
NC_000008.10:g.58986459G>A , CM000670.1:g.58986459G>A GRCh37
NC_000008.9:g.59149013G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361488.7:c.-413-1635G>A ENSP00000355204.3:p.=
ENST00000518427.5:n.182-1635G>A
ENST00000519262.5:n.397-1635G>A
ENST00000520369.5:n.338-1635G>A
ENST00000521413.1:n.46-1635G>A
ENST00000522059.5:n.89-1635G>A
ENST00000523486.5:n.137-1635G>A
NM_147189.2:c.-413-1635G>A NP_671722.1:p.=
XM_005251324.1:c.-413-1635G>A XP_005251381.1:p.=
XM_005251325.2:c.-413-1635G>A XP_005251382.1:p.=
XM_005251326.1:c.-413-1635G>A XP_005251383.1:p.=
XM_005251324.3:c.-413-1635G>A XP_005251381.1:p.=
XM_005251325.3:c.-413-1635G>A XP_005251382.1:p.=
XM_005251326.3:c.-413-1635G>A XP_005251383.1:p.=
XM_017013948.1:c.-413-1635G>A XP_016869437.1:p.=
NM_147189.3:c.-413-1635G>A NP_671722.1:p.=
NM_001377989.1:c.-413-1635G>A NP_001364918.1:p.=
NM_001377997.1:c.-413-1635G>A NP_001364926.1:p.=
NM_001377998.1:c.-413-1635G>A NP_001364927.1:p.=
NM_147189.4:c.-413-1635G>A NP_671722.1:p.=