Canonical Allele Identifier: CA351807695

Gene: TGFBR2

Linked Data

• gnomAD v4: 3-30671890-A-G
• MyVariant Identifiers: chr3:g.30713382A>G (hg19) ; chr3:g.30671890A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671890A>G , CM000665.2:g.30671890A>G	GRCh38
NC_000003.11:g.30713382A>G , CM000665.1:g.30713382A>G	GRCh37
NC_000003.10:g.30688386A>G	NCBI36
NG_007490.1:g.70389A>G , LRG_779:g.70389A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.707A>G MANE Select	ENSP00000295754.5:p.Asn236Ser
ENST00000672866.1:n.2303A>G
ENST00000295754.9:c.707A>G	ENSP00000295754.5:p.Asn236Ser
ENST00000359013.4:c.782A>G	ENSP00000351905.4:p.Asn261Ser
NM_001024847.2:c.782A>G , LRG_779t1:c.782A>G	NP_001020018.1:p.Asn261Ser
NM_003242.5:c.707A>G	NP_003233.4:p.Asn236Ser
XM_011534043.1:c.734A>G	XP_011532345.1:p.Asn245Ser
XM_011534044.1:c.659A>G	XP_011532346.1:p.Asn220Ser
XM_011534045.1:c.602A>G	XP_011532347.1:p.Asn201Ser
XM_011534043.2:c.734A>G	XP_011532345.1:p.Asn245Ser
XM_011534045.3:c.602A>G	XP_011532347.1:p.Asn201Ser
XM_017007106.1:c.602A>G	XP_016862595.1:p.Asn201Ser
NM_003242.6:c.707A>G MANE Select	NP_003233.4:p.Asn236Ser