Canonical Allele Identifier: CA2007037443

Gene: FAM118B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126222046C= , CM000673.2:g.126222046C=	GRCh38
NC_000011.9:g.126091941C= , CM000673.1:g.126091941C=	GRCh37
NC_000011.8:g.125597151C=	NCBI36
NG_017156.1:g.15323C=

Transcript Alleles

HGVS	Amino-acid Change
NM_024556.4:c.-76-7179C= MANE Select	NP_078832.1:n.-76-7179C=
ENST00000533050.6:c.-76-7179C= MANE Select	ENSP00000433343.1:n.-76-7179C=
NM_001330446.1:c.-76-7179C=	NP_001317375.1:n.-76-7179C=
NM_024556.3:c.-76-7179C=	NP_078832.1:n.-76-7179C=
ENST00000360194.8:c.-8+10216C=	ENSP00000353321.4:n.-8+10216C=
ENST00000525728.5:n.66-7179C=
ENST00000528985.5:c.-212-7179C=	ENSP00000434952.1:n.-212-7179C=
ENST00000529731.5:c.-8+10216C=	ENSP00000432712.1:n.-8+10216C=
ENST00000530043.5:c.-119-7179C=	ENSP00000437285.1:n.-119-7179C=
ENST00000533050.5:c.-76-7179C=	ENSP00000433343.1:n.-76-7179C=
ENST00000627851.2:c.-76-7179C=	ENSP00000487554.1:n.-76-7179C=
XM_005271665.2:c.-76-7179C=	XP_005271722.1:n.-76-7179C=
XM_011542977.1:c.-8+10216C=	XP_011541279.1:n.-8+10216C=
XM_011542977.3:c.-8+10216C=	XP_011541279.1:n.-8+10216C=
XM_011542978.1:c.-587-7179C=	XP_011541280.1:n.-587-7179C=
XM_011542978.3:c.-587-7179C=	XP_011541280.1:n.-587-7179C=
XM_011542979.1:c.-519+10216C=	XP_011541281.1:n.-519+10216C=
XM_017018285.2:c.-8+10216C=	XP_016873774.1:n.-8+10216C=
XM_017018286.1:c.-587-7179C=	XP_016873775.1:n.-587-7179C=