Canonical Allele Identifier: CA906181270

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1408235127
• gnomAD v3: 3-30617076-T-G
• gnomAD v4: 3-30617076-T-G
• MyVariant Identifiers: chr3:g.30658568T>G (hg19) ; chr3:g.30617076T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30617076T>G , CM000665.2:g.30617076T>G	GRCh38
NC_000003.11:g.30658568T>G , CM000665.1:g.30658568T>G	GRCh37
NC_000003.10:g.30633572T>G	NCBI36
NG_007490.1:g.15575T>G , LRG_779:g.15575T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10099T>G MANE Select	ENSP00000295754.5:n.94+10099T>G
ENST00000673250.1:n.143+2370T>G
ENST00000295754.9:c.94+10099T>G	ENSP00000295754.5:n.94+10099T>G
ENST00000359013.4:c.95-6123T>G	ENSP00000351905.4:n.95-6123T>G
NM_001024847.2:c.95-6123T>G , LRG_779t1:c.95-6123T>G	NP_001020018.1:n.95-6123T>G
NM_003242.5:c.94+10099T>G	NP_003233.4:n.94+10099T>G
XM_011534043.1:c.46+2370T>G	XP_011532345.1:n.46+2370T>G
XM_011534044.1:c.46+2370T>G	XP_011532346.1:n.46+2370T>G
XM_011534045.1:c.-12+10483T>G	XP_011532347.1:n.-12+10483T>G
XM_011534043.2:c.46+2370T>G	XP_011532345.1:n.46+2370T>G
XM_011534045.3:c.-12+10483T>G	XP_011532347.1:n.-12+10483T>G
NM_003242.6:c.94+10099T>G MANE Select	NP_003233.4:n.94+10099T>G