Canonical Allele Identifier: CA3862793

Gene: FAM83B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.54926424C>T , CM000668.2:g.54926424C>T	GRCh38
NC_000006.11:g.54791222C>T , CM000668.1:g.54791222C>T	GRCh37
NC_000006.10:g.54899181C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001010872.3:c.498C>T MANE Select	NP_001010872.1:p.Ile166=
ENST00000306858.8:c.498C>T MANE Select	ENSP00000304078.7:p.Ile166=
NM_001010872.2:c.498C>T	NP_001010872.1:p.Ile166=
ENST00000306858.7:c.498C>T	ENSP00000304078.7:p.Ile166=
XM_006715022.2:c.498C>T	XP_006715085.1:p.Ile166=
XM_006715022.3:c.498C>T	XP_006715085.1:p.Ile166=
XM_011514394.1:c.498C>T	XP_011512696.1:p.Ile166=
XM_011514394.2:c.498C>T	XP_011512696.1:p.Ile166=
XM_011514395.1:c.498C>T	XP_011512697.1:p.Ile166=
XM_011514395.2:c.498C>T	XP_011512697.1:p.Ile166=
XM_017010478.1:c.498C>T	XP_016865967.1:p.Ile166=