Canonical Allele Identifier: CA1046445416

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1697929623
• gnomAD v3: 3-30606792-A-G
• gnomAD v4: 3-30606792-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606792A>G , CM000665.2:g.30606792A>G	GRCh38
NC_000003.11:g.30648284A>G , CM000665.1:g.30648284A>G	GRCh37
NC_000003.10:g.30623288A>G	NCBI36
NG_007490.1:g.5291A>G , LRG_779:g.5291A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.-92A>G MANE Select	ENSP00000295754.5:n.-92A>G
ENST00000295754.9:c.-92A>G	ENSP00000295754.5:n.-92A>G
ENST00000359013.4:c.-92A>G	ENSP00000351905.4:n.-92A>G
NM_001024847.2:c.-92A>G , LRG_779t1:c.-92A>G	NP_001020018.1:n.-92A>G
NM_003242.5:c.-92A>G	NP_003233.4:n.-92A>G
XM_011534045.1:c.-12+199A>G	XP_011532347.1:n.-12+199A>G
XM_011534045.3:c.-12+199A>G	XP_011532347.1:n.-12+199A>G
NM_003242.6:c.-92A>G MANE Select	NP_003233.4:n.-92A>G