Canonical Allele Identifier: CA351830498

Gene: TGFBR2

Linked Data

• gnomAD v4: 3-30606906-G-T
• MyVariant Identifiers: chr3:g.30648398G>T (hg19) ; chr3:g.30606906G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606906G>T , CM000665.2:g.30606906G>T	GRCh38
NC_000003.11:g.30648398G>T , CM000665.1:g.30648398G>T	GRCh37
NC_000003.10:g.30623402G>T	NCBI36
NG_007490.1:g.5405G>T , LRG_779:g.5405G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.23G>T MANE Select	ENSP00000295754.5:p.Gly8Val
ENST00000295754.9:c.23G>T	ENSP00000295754.5:p.Gly8Val
ENST00000359013.4:c.23G>T	ENSP00000351905.4:p.Gly8Val
NM_001024847.2:c.23G>T , LRG_779t1:c.23G>T	NP_001020018.1:p.Gly8Val
NM_003242.5:c.23G>T	NP_003233.4:p.Gly8Val
XM_011534045.1:c.-12+313G>T	XP_011532347.1:n.-12+313G>T
XM_011534045.3:c.-12+313G>T	XP_011532347.1:n.-12+313G>T
NM_003242.6:c.23G>T MANE Select	NP_003233.4:p.Gly8Val