Canonical Allele Identifier: CA13473755

Gene: FAM118B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126231037C>T , CM000673.2:g.126231037C>T	GRCh38
NC_000011.9:g.126100932C>T , CM000673.1:g.126100932C>T	GRCh37
NC_000011.8:g.125606142C>T	NCBI36
NG_017156.1:g.24314C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000533050.6:c.-8+1744C>T MANE Select	ENSP00000433343.1:n.-8+1744C>T
ENST00000360194.8:c.-7-3958C>T	ENSP00000353321.4:n.-7-3958C>T
ENST00000525338.1:c.-8+1744C>T	ENSP00000435754.1:n.-8+1744C>T
ENST00000525728.5:n.134+1744C>T
ENST00000527247.5:n.70+1744C>T
ENST00000528985.5:c.-144+1744C>T	ENSP00000434952.1:n.-144+1744C>T
ENST00000529731.5:c.-7-3958C>T	ENSP00000432712.1:n.-7-3958C>T
ENST00000530043.5:c.-8+1701C>T	ENSP00000437285.1:n.-8+1701C>T
ENST00000533050.5:c.-8+1744C>T	ENSP00000433343.1:n.-8+1744C>T
ENST00000627851.2:c.-8+1744C>T	ENSP00000487554.1:n.-8+1744C>T
NM_024556.3:c.-8+1744C>T	NP_078832.1:n.-8+1744C>T
XM_005271665.2:c.-8+1744C>T	XP_005271722.1:n.-8+1744C>T
XM_011542977.1:c.-7-3958C>T	XP_011541279.1:n.-7-3958C>T
XM_011542978.1:c.-519+1744C>T	XP_011541280.1:n.-519+1744C>T
XM_011542979.1:c.-518-3958C>T	XP_011541281.1:n.-518-3958C>T
NM_001330446.1:c.-8+1744C>T	NP_001317375.1:n.-8+1744C>T
XM_011542977.3:c.-7-3958C>T	XP_011541279.1:n.-7-3958C>T
XM_011542978.3:c.-519+1744C>T	XP_011541280.1:n.-519+1744C>T
XM_017018285.2:c.-7-3958C>T	XP_016873774.1:n.-7-3958C>T
XM_017018286.1:c.-519+1744C>T	XP_016873775.1:n.-519+1744C>T
NM_024556.4:c.-8+1744C>T MANE Select	NP_078832.1:n.-8+1744C>T