Canonical Allele Identifier: CA740329894

Gene: TGFBR3

Linked Data

• dbSNP Id: rs1335563572
• gnomAD v3: 1-91866936-G-C
• gnomAD v4: 1-91866936-G-C
• MyVariant Identifiers: chr1:g.92332493G>C (hg19) ; chr1:g.91866936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91866936G>C , CM000663.2:g.91866936G>C	GRCh38
NC_000001.10:g.92332493G>C , CM000663.1:g.92332493G>C	GRCh37
NC_000001.9:g.92105081G>C	NCBI36
NG_027757.1:g.44067C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000212355.9:c.-113-5292C>G MANE Select	ENSP00000212355.4:n.-113-5292C>G
ENST00000212355.8:c.-113-5292C>G	ENSP00000212355.4:n.-113-5292C>G
ENST00000370399.6:c.-113-5292C>G	ENSP00000359426.2:n.-113-5292C>G
ENST00000417833.2:c.-200-94C>G	ENSP00000395975.2:n.-200-94C>G
ENST00000465892.6:c.-113-5292C>G	ENSP00000432638.1:n.-113-5292C>G
ENST00000532540.5:c.-113-5292C>G	ENSP00000434994.1:n.-113-5292C>G
ENST00000533370.1:n.123-2657C>G
NM_001195683.1:c.-113-5292C>G	NP_001182612.1:n.-113-5292C>G
NM_001195684.1:c.-113-5292C>G	NP_001182613.1:n.-113-5292C>G
NM_003243.4:c.-113-5292C>G	NP_003234.2:n.-113-5292C>G
NR_036634.1:n.403-5292C>G
XM_006710867.1:c.-113-5292C>G	XP_006710930.1:n.-113-5292C>G
XM_006710867.2:c.-113-5292C>G	XP_006710930.1:n.-113-5292C>G
NM_003243.5:c.-113-5292C>G MANE Select	NP_003234.2:n.-113-5292C>G
NM_001195683.2:c.-113-5292C>G	NP_001182612.1:n.-113-5292C>G
NR_036634.2:n.275-5292C>G