Canonical Allele Identifier: CA6352967

Gene: FAM118B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126240846T>G , CM000673.2:g.126240846T>G	GRCh38
NC_000011.9:g.126110741T>G , CM000673.1:g.126110741T>G	GRCh37
NC_000011.8:g.125615951T>G	NCBI36
NG_017156.1:g.34123T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000533050.6:c.141T>G MANE Select	ENSP00000433343.1:p.Ile47Met
ENST00000360194.8:c.141T>G	ENSP00000353321.4:p.Ile47Met
ENST00000525338.1:c.141T>G	ENSP00000435754.1:p.Ile47Met
ENST00000525728.5:n.189T>G
ENST00000527247.5:n.218T>G
ENST00000528985.5:c.141T>G	ENSP00000434952.1:p.Ile47Met
ENST00000529731.5:c.141T>G	ENSP00000432712.1:p.Ile47Met
ENST00000530043.5:c.141T>G	ENSP00000437285.1:p.Ile47Met
ENST00000533050.5:c.141T>G	ENSP00000433343.1:p.Ile47Met
ENST00000627851.2:c.141T>G	ENSP00000487554.1:p.Ile47Met
NM_024556.3:c.141T>G	NP_078832.1:p.Ile47Met
XM_005271665.2:c.141T>G	XP_005271722.1:p.Ile47Met
XM_011542977.1:c.141T>G	XP_011541279.1:p.Ile47Met
XM_011542978.1:c.-371T>G	XP_011541280.1:n.-371T>G
XM_011542979.1:c.-371T>G	XP_011541281.1:n.-371T>G
NM_001330446.1:c.141T>G	NP_001317375.1:p.Ile47Met
XM_011542977.3:c.141T>G	XP_011541279.1:p.Ile47Met
XM_011542978.3:c.-371T>G	XP_011541280.1:n.-371T>G
XM_017018285.2:c.141T>G	XP_016873774.1:p.Ile47Met
XM_017018286.1:c.-371T>G	XP_016873775.1:n.-371T>G
NM_024556.4:c.141T>G MANE Select	NP_078832.1:p.Ile47Met