Canonical Allele Identifier: CA2843544767

Gene: FAM110B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58073962A>G , CM000670.2:g.58073962A>G	GRCh38
NC_000008.10:g.58986521A>G , CM000670.1:g.58986521A>G	GRCh37
NC_000008.9:g.59149075A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519262.6:c.-413-1573A>G MANE Select	ENSP00000509301.1:n.-413-1573A>G
ENST00000361488.7:c.-413-1573A>G	ENSP00000355204.3:n.-413-1573A>G
ENST00000518427.5:n.182-1573A>G
ENST00000519262.5:n.397-1573A>G
ENST00000520369.5:n.338-1573A>G
ENST00000521413.1:n.46-1573A>G
ENST00000522059.5:n.89-1573A>G
ENST00000523486.5:n.137-1573A>G
NM_147189.2:c.-413-1573A>G	NP_671722.1:n.-413-1573A>G
XM_005251324.1:c.-413-1573A>G	XP_005251381.1:n.-413-1573A>G
XM_005251325.2:c.-413-1573A>G	XP_005251382.1:n.-413-1573A>G
XM_005251326.1:c.-413-1573A>G	XP_005251383.1:n.-413-1573A>G
XM_005251324.3:c.-413-1573A>G	XP_005251381.1:n.-413-1573A>G
XM_005251325.3:c.-413-1573A>G	XP_005251382.1:n.-413-1573A>G
XM_005251326.3:c.-413-1573A>G	XP_005251383.1:n.-413-1573A>G
XM_017013948.1:c.-413-1573A>G	XP_016869437.1:n.-413-1573A>G
NM_147189.3:c.-413-1573A>G	NP_671722.1:n.-413-1573A>G
NM_001377989.1:c.-413-1573A>G MANE Select	NP_001364918.1:n.-413-1573A>G
NM_001377997.1:c.-413-1573A>G	NP_001364926.1:n.-413-1573A>G
NM_001377998.1:c.-413-1573A>G	NP_001364927.1:n.-413-1573A>G
NM_147189.4:c.-413-1573A>G	NP_671722.1:n.-413-1573A>G