Canonical Allele Identifier: CA1786790372

Gene: FAM110B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58073882T= , CM000670.2:g.58073882T=	GRCh38
NC_000008.10:g.58986441T= , CM000670.1:g.58986441T=	GRCh37
NC_000008.9:g.59148995T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519262.6:c.-413-1653T= MANE Select	ENSP00000509301.1:n.-413-1653T=
ENST00000361488.7:c.-413-1653T=	ENSP00000355204.3:n.-413-1653T=
ENST00000518427.5:n.182-1653T=
ENST00000519262.5:n.397-1653T=
ENST00000520369.5:n.338-1653T=
ENST00000521413.1:n.46-1653T=
ENST00000522059.5:n.89-1653T=
ENST00000523486.5:n.137-1653T=
NM_147189.2:c.-413-1653T=	NP_671722.1:n.-413-1653T=
XM_005251324.1:c.-413-1653T=	XP_005251381.1:n.-413-1653T=
XM_005251325.2:c.-413-1653T=	XP_005251382.1:n.-413-1653T=
XM_005251326.1:c.-413-1653T=	XP_005251383.1:n.-413-1653T=
XM_005251324.3:c.-413-1653T=	XP_005251381.1:n.-413-1653T=
XM_005251325.3:c.-413-1653T=	XP_005251382.1:n.-413-1653T=
XM_005251326.3:c.-413-1653T=	XP_005251383.1:n.-413-1653T=
XM_017013948.1:c.-413-1653T=	XP_016869437.1:n.-413-1653T=
NM_147189.3:c.-413-1653T=	NP_671722.1:n.-413-1653T=
NM_001377989.1:c.-413-1653T= MANE Select	NP_001364918.1:n.-413-1653T=
NM_001377997.1:c.-413-1653T=	NP_001364926.1:n.-413-1653T=
NM_001377998.1:c.-413-1653T=	NP_001364927.1:n.-413-1653T=
NM_147189.4:c.-413-1653T=	NP_671722.1:n.-413-1653T=