Canonical Allele Identifier: CA2646555219

Gene: TGFBR3

Linked Data

• gnomAD v4: 1-91866943-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91866943G>T , CM000663.2:g.91866943G>T	GRCh38
NC_000001.10:g.92332500G>T , CM000663.1:g.92332500G>T	GRCh37
NC_000001.9:g.92105088G>T	NCBI36
NG_027757.1:g.44060C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212355.9:c.-113-5299C>A MANE Select	ENSP00000212355.4:n.-113-5299C>A
ENST00000212355.8:c.-113-5299C>A	ENSP00000212355.4:n.-113-5299C>A
ENST00000370399.6:c.-113-5299C>A	ENSP00000359426.2:n.-113-5299C>A
ENST00000417833.2:c.-200-101C>A	ENSP00000395975.2:n.-200-101C>A
ENST00000465892.6:c.-113-5299C>A	ENSP00000432638.1:n.-113-5299C>A
ENST00000532540.5:c.-113-5299C>A	ENSP00000434994.1:n.-113-5299C>A
ENST00000533370.1:n.123-2664C>A
NM_001195683.1:c.-113-5299C>A	NP_001182612.1:n.-113-5299C>A
NM_001195684.1:c.-113-5299C>A	NP_001182613.1:n.-113-5299C>A
NM_003243.4:c.-113-5299C>A	NP_003234.2:n.-113-5299C>A
NR_036634.1:n.403-5299C>A
XM_006710867.1:c.-113-5299C>A	XP_006710930.1:n.-113-5299C>A
XM_006710867.2:c.-113-5299C>A	XP_006710930.1:n.-113-5299C>A
NM_003243.5:c.-113-5299C>A MANE Select	NP_003234.2:n.-113-5299C>A
NM_001195683.2:c.-113-5299C>A	NP_001182612.1:n.-113-5299C>A
NR_036634.2:n.275-5299C>A