Canonical Allele Identifier: CA2646555223

Gene: TGFBR3

Linked Data

• gnomAD v4: 1-91866953-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91866953A>G , CM000663.2:g.91866953A>G	GRCh38
NC_000001.10:g.92332510A>G , CM000663.1:g.92332510A>G	GRCh37
NC_000001.9:g.92105098A>G	NCBI36
NG_027757.1:g.44050T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000212355.9:c.-113-5309T>C MANE Select	ENSP00000212355.4:n.-113-5309T>C
ENST00000212355.8:c.-113-5309T>C	ENSP00000212355.4:n.-113-5309T>C
ENST00000370399.6:c.-113-5309T>C	ENSP00000359426.2:n.-113-5309T>C
ENST00000417833.2:c.-200-111T>C	ENSP00000395975.2:n.-200-111T>C
ENST00000465892.6:c.-113-5309T>C	ENSP00000432638.1:n.-113-5309T>C
ENST00000532540.5:c.-113-5309T>C	ENSP00000434994.1:n.-113-5309T>C
ENST00000533370.1:n.123-2674T>C
NM_001195683.1:c.-113-5309T>C	NP_001182612.1:n.-113-5309T>C
NM_001195684.1:c.-113-5309T>C	NP_001182613.1:n.-113-5309T>C
NM_003243.4:c.-113-5309T>C	NP_003234.2:n.-113-5309T>C
NR_036634.1:n.403-5309T>C
XM_006710867.1:c.-113-5309T>C	XP_006710930.1:n.-113-5309T>C
XM_006710867.2:c.-113-5309T>C	XP_006710930.1:n.-113-5309T>C
NM_003243.5:c.-113-5309T>C MANE Select	NP_003234.2:n.-113-5309T>C
NM_001195683.2:c.-113-5309T>C	NP_001182612.1:n.-113-5309T>C
NR_036634.2:n.275-5309T>C