Canonical Allele Identifier: CA351808450

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125435833
• gnomAD v4: 3-30672238-G-A
• MyVariant Identifiers: chr3:g.30713730G>A (hg19) ; chr3:g.30672238G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672238G>A , CM000665.2:g.30672238G>A	GRCh38
NC_000003.11:g.30713730G>A , CM000665.1:g.30713730G>A	GRCh37
NC_000003.10:g.30688734G>A	NCBI36
NG_007490.1:g.70737G>A , LRG_779:g.70737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1055G>A MANE Select	ENSP00000295754.5:p.Ser352Asn
ENST00000672866.1:n.2651G>A
ENST00000295754.9:c.1055G>A	ENSP00000295754.5:p.Ser352Asn
ENST00000359013.4:c.1130G>A	ENSP00000351905.4:p.Ser377Asn
NM_001024847.2:c.1130G>A , LRG_779t1:c.1130G>A	NP_001020018.1:p.Ser377Asn
NM_003242.5:c.1055G>A	NP_003233.4:p.Ser352Asn
XM_011534043.1:c.1082G>A	XP_011532345.1:p.Ser361Asn
XM_011534044.1:c.1007G>A	XP_011532346.1:p.Ser336Asn
XM_011534045.1:c.950G>A	XP_011532347.1:p.Ser317Asn
XM_011534043.2:c.1082G>A	XP_011532345.1:p.Ser361Asn
XM_011534045.3:c.950G>A	XP_011532347.1:p.Ser317Asn
XM_017007106.1:c.950G>A	XP_016862595.1:p.Ser317Asn
NM_003242.6:c.1055G>A MANE Select	NP_003233.4:p.Ser352Asn