Canonical Allele Identifier: CA186478355

Gene: FAM135B

Linked Data

• dbSNP Id: rs10875423
• MyVariant Identifiers: chr8:g.139301378T>G (hg19) ; chr8:g.138289135T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138289135T>G , CM000670.2:g.138289135T>G	GRCh38
NC_000008.10:g.139301378T>G , CM000670.1:g.139301378T>G	GRCh37
NC_000008.9:g.139370560T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395297.6:c.157+21706A>C MANE Select	ENSP00000378710.1:n.157+21706A>C
ENST00000160713.8:c.157+21706A>C	ENSP00000160713.4:n.157+21706A>C
ENST00000276737.10:c.157+21706A>C	ENSP00000276737.6:n.157+21706A>C
ENST00000395297.5:c.157+21706A>C	ENSP00000378710.1:n.157+21706A>C
ENST00000482951.6:c.*103+21706A>C	ENSP00000429874.1:n.*103+21706A>C
ENST00000517849.1:n.523+21706A>C
NM_015912.3:c.157+21706A>C	NP_056996.2:n.157+21706A>C
XM_011517056.1:c.157+21706A>C	XP_011515358.1:n.157+21706A>C
XM_011517057.1:c.157+21706A>C	XP_011515359.1:n.157+21706A>C
XM_011517058.1:c.157+21706A>C	XP_011515360.1:n.157+21706A>C
XM_011517059.1:c.157+21706A>C	XP_011515361.1:n.157+21706A>C
XM_011517060.1:c.157+21706A>C	XP_011515362.1:n.157+21706A>C
XM_011517061.1:c.157+21706A>C	XP_011515363.1:n.157+21706A>C
XM_011517062.1:c.157+21706A>C	XP_011515364.1:n.157+21706A>C
XM_011517063.1:c.157+21706A>C	XP_011515365.1:n.157+21706A>C
XM_011517064.1:c.157+21706A>C	XP_011515366.1:n.157+21706A>C
XM_011517065.1:c.109+21706A>C	XP_011515367.1:n.109+21706A>C
XM_011517066.1:c.157+21706A>C	XP_011515368.1:n.157+21706A>C
XM_011517067.1:c.157+21706A>C	XP_011515369.1:n.157+21706A>C
XM_011517068.1:c.-141+21706A>C	XP_011515370.1:n.-141+21706A>C
XM_011517070.1:c.157+21706A>C	XP_011515372.1:n.157+21706A>C
XM_011517071.1:c.157+21706A>C	XP_011515373.1:n.157+21706A>C
NM_001362965.1:c.157+21706A>C	NP_001349894.1:n.157+21706A>C
XM_011517056.2:c.157+21706A>C	XP_011515358.1:n.157+21706A>C
XM_011517058.2:c.157+21706A>C	XP_011515360.1:n.157+21706A>C
XM_011517060.2:c.157+21706A>C	XP_011515362.1:n.157+21706A>C
XM_011517061.2:c.157+21706A>C	XP_011515363.1:n.157+21706A>C
XM_011517063.2:c.157+21706A>C	XP_011515365.1:n.157+21706A>C
XM_011517064.2:c.157+21706A>C	XP_011515366.1:n.157+21706A>C
XM_011517068.2:c.-141+21706A>C	XP_011515370.1:n.-141+21706A>C
XM_011517070.2:c.157+21706A>C	XP_011515372.1:n.157+21706A>C
XM_017013471.1:c.157+21706A>C	XP_016868960.1:n.157+21706A>C
XR_001745531.1:n.1136+21706A>C
XR_001745532.1:n.1137+21706A>C
NM_015912.4:c.157+21706A>C MANE Select	NP_056996.2:n.157+21706A>C
NM_001362965.2:c.157+21706A>C	NP_001349894.1:n.157+21706A>C