Canonical Allele Identifier: CA906173492

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1349717097
• gnomAD v4: 3-30606833-C-G
• MyVariant Identifiers: chr3:g.30648325C>G (hg19) ; chr3:g.30606833C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606833C>G , CM000665.2:g.30606833C>G	GRCh38
NC_000003.11:g.30648325C>G , CM000665.1:g.30648325C>G	GRCh37
NC_000003.10:g.30623329C>G	NCBI36
NG_007490.1:g.5332C>G , LRG_779:g.5332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.-51C>G MANE Select	ENSP00000295754.5:n.-51C>G
ENST00000295754.9:c.-51C>G	ENSP00000295754.5:n.-51C>G
ENST00000359013.4:c.-51C>G	ENSP00000351905.4:n.-51C>G
NM_001024847.2:c.-51C>G , LRG_779t1:c.-51C>G	NP_001020018.1:n.-51C>G
NM_003242.5:c.-51C>G	NP_003233.4:n.-51C>G
XM_011534045.1:c.-12+240C>G	XP_011532347.1:n.-12+240C>G
XM_011534045.3:c.-12+240C>G	XP_011532347.1:n.-12+240C>G
NM_003242.6:c.-51C>G MANE Select	NP_003233.4:n.-51C>G