Canonical Allele Identifier: CA906197382

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1329605582
• gnomAD v3: 3-30649503-A-G
• gnomAD v4: 3-30649503-A-G
• MyVariant Identifiers: chr3:g.30690995A>G (hg19) ; chr3:g.30649503A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649503A>G , CM000665.2:g.30649503A>G	GRCh38
NC_000003.11:g.30690995A>G , CM000665.1:g.30690995A>G	GRCh37
NC_000003.10:g.30665999A>G	NCBI36
NG_007490.1:g.48002A>G , LRG_779:g.48002A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-767A>G MANE Select	ENSP00000295754.5:n.264-767A>G
ENST00000672866.1:n.1860-767A>G
ENST00000673250.1:n.388-767A>G
ENST00000295754.9:c.264-767A>G	ENSP00000295754.5:n.264-767A>G
ENST00000359013.4:c.339-767A>G	ENSP00000351905.4:n.339-767A>G
NM_001024847.2:c.339-767A>G , LRG_779t1:c.339-767A>G	NP_001020018.1:n.339-767A>G
NM_003242.5:c.264-767A>G	NP_003233.4:n.264-767A>G
XM_011534043.1:c.291-767A>G	XP_011532345.1:n.291-767A>G
XM_011534044.1:c.216-767A>G	XP_011532346.1:n.216-767A>G
XM_011534045.1:c.159-767A>G	XP_011532347.1:n.159-767A>G
XM_011534043.2:c.291-767A>G	XP_011532345.1:n.291-767A>G
XM_011534045.3:c.159-767A>G	XP_011532347.1:n.159-767A>G
XM_017007106.1:c.159-767A>G	XP_016862595.1:n.159-767A>G
NM_003242.6:c.264-767A>G MANE Select	NP_003233.4:n.264-767A>G