Canonical Allele Identifier: CA2664866657

Gene: TGFBR2

Linked Data

• gnomAD v4: 3-30606799-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606799G>C , CM000665.2:g.30606799G>C	GRCh38
NC_000003.11:g.30648291G>C , CM000665.1:g.30648291G>C	GRCh37
NC_000003.10:g.30623295G>C	NCBI36
NG_007490.1:g.5298G>C , LRG_779:g.5298G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.-85G>C MANE Select	ENSP00000295754.5:n.-85G>C
ENST00000295754.9:c.-85G>C	ENSP00000295754.5:n.-85G>C
ENST00000359013.4:c.-85G>C	ENSP00000351905.4:n.-85G>C
NM_001024847.2:c.-85G>C , LRG_779t1:c.-85G>C	NP_001020018.1:n.-85G>C
NM_003242.5:c.-85G>C	NP_003233.4:n.-85G>C
XM_011534045.1:c.-12+206G>C	XP_011532347.1:n.-12+206G>C
XM_011534045.3:c.-12+206G>C	XP_011532347.1:n.-12+206G>C
NM_003242.6:c.-85G>C MANE Select	NP_003233.4:n.-85G>C