Canonical Allele Identifier: CA2390271115

Gene: FAM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41327116G= , CM000683.2:g.41327116G=	GRCh38
NC_000021.8:g.42699043G= , CM000683.1:g.42699043G=	GRCh37
NC_000021.7:g.41620913G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357985.7:c.163+4050G= MANE Select	ENSP00000350673.2:n.163+4050G=
ENST00000357985.6:c.163+4050G=	ENSP00000350673.2:n.163+4050G=
ENST00000398646.3:c.232+4050G=	ENSP00000381641.3:n.232+4050G=
ENST00000398647.7:c.19+10218G=	ENSP00000381642.3:n.19+10218G=
ENST00000398652.7:c.280+4050G=	ENSP00000381646.3:n.280+4050G=
ENST00000479810.6:n.1764+4050G=
ENST00000518236.1:n.205+4050G=
NM_058186.3:c.163+4050G=	NP_478066.3:n.163+4050G=
NM_206964.1:c.19+10218G=	NP_996847.1:n.19+10218G=
XM_011529648.1:c.163+4050G=	XP_011527950.1:n.163+4050G=
XM_011529649.1:c.205+4050G=	XP_011527951.1:n.205+4050G=
XR_937526.1:n.662+4050G=
XM_011529648.2:c.391+4050G=	XP_011527950.2:n.391+4050G=
XM_011529649.2:c.205+4050G=	XP_011527951.1:n.205+4050G=
XR_937526.2:n.663+4050G=
NM_058186.4:c.163+4050G= MANE Select	NP_478066.3:n.163+4050G=
NM_206964.2:c.19+10218G=	NP_996847.1:n.19+10218G=