Canonical Allele Identifier: CA72291148

Gene: TGFBR2

Linked Data

• dbSNP Id: rs34626019
• gnomAD v3: 3-30617083-A-G
• gnomAD v4: 3-30617083-A-G
• COSMIC: COSN25932852 ; COSN25945809 ; COSN26013851
• MyVariant Identifiers: chr3:g.30658575A>G (hg19) ; chr3:g.30617083A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30617083A>G , CM000665.2:g.30617083A>G	GRCh38
NC_000003.11:g.30658575A>G , CM000665.1:g.30658575A>G	GRCh37
NC_000003.10:g.30633579A>G	NCBI36
NG_007490.1:g.15582A>G , LRG_779:g.15582A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10106A>G MANE Select	ENSP00000295754.5:n.94+10106A>G
ENST00000673250.1:n.143+2377A>G
ENST00000295754.9:c.94+10106A>G	ENSP00000295754.5:n.94+10106A>G
ENST00000359013.4:c.95-6116A>G	ENSP00000351905.4:n.95-6116A>G
NM_001024847.2:c.95-6116A>G , LRG_779t1:c.95-6116A>G	NP_001020018.1:n.95-6116A>G
NM_003242.5:c.94+10106A>G	NP_003233.4:n.94+10106A>G
XM_011534043.1:c.46+2377A>G	XP_011532345.1:n.46+2377A>G
XM_011534044.1:c.46+2377A>G	XP_011532346.1:n.46+2377A>G
XM_011534045.1:c.-12+10490A>G	XP_011532347.1:n.-12+10490A>G
XM_011534043.2:c.46+2377A>G	XP_011532345.1:n.46+2377A>G
XM_011534045.3:c.-12+10490A>G	XP_011532347.1:n.-12+10490A>G
NM_003242.6:c.94+10106A>G MANE Select	NP_003233.4:n.94+10106A>G