Canonical Allele Identifier: CA56902214

Gene: THSD7B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137011132A>C , CM000664.2:g.137011132A>C	GRCh38
NC_000002.11:g.137768702A>C , CM000664.1:g.137768702A>C	GRCh37
NC_000002.10:g.137485172A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409968.6:c.140-45288A>C MANE Select	ENSP00000387145.1:n.140-45288A>C
ENST00000272643.7:c.140-45288A>C	ENSP00000272643.4:n.140-45288A>C
ENST00000409968.5:c.140-45288A>C	ENSP00000387145.1:n.140-45288A>C
ENST00000413152.3:c.46+20195A>C	ENSP00000413841.3:n.46+20195A>C
ENST00000472720.5:c.*106-45288A>C	ENSP00000473349.1:n.*106-45288A>C
NM_001080427.1:c.46+20195A>C	NP_001073896.1:n.46+20195A>C
NM_001316349.1:c.140-45288A>C	NP_001303278.1:n.140-45288A>C
NM_001316349.2:c.140-45288A>C MANE Select	NP_001303278.1:n.140-45288A>C