Canonical Allele Identifier: CA12945218

Gene: FAM135B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138492027C>T , CM000670.2:g.138492027C>T	GRCh38
NC_000008.10:g.139504270C>T , CM000670.1:g.139504270C>T	GRCh37
NC_000008.9:g.139573452C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395297.6:c.-20+4644G>A MANE Select	ENSP00000378710.1:n.-20+4644G>A
ENST00000276737.10:c.-20+4644G>A	ENSP00000276737.6:n.-20+4644G>A
ENST00000395297.5:c.-20+4644G>A	ENSP00000378710.1:n.-20+4644G>A
NM_015912.3:c.-20+4644G>A	NP_056996.2:n.-20+4644G>A
XM_011517061.1:c.-165+4644G>A	XP_011515363.1:n.-165+4644G>A
XM_011517062.1:c.-20+4644G>A	XP_011515364.1:n.-20+4644G>A
NM_001362965.1:c.-20+5600G>A	NP_001349894.1:n.-20+5600G>A
XM_011517061.2:c.-165+4644G>A	XP_011515363.1:n.-165+4644G>A
NM_015912.4:c.-20+4644G>A MANE Select	NP_056996.2:n.-20+4644G>A
NM_001362965.2:c.-20+5600G>A	NP_001349894.1:n.-20+5600G>A