Canonical Allele Identifier: CA2664866748

Gene: TGFBR2

Linked Data

• gnomAD v4: 3-30606880-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606880T>C , CM000665.2:g.30606880T>C	GRCh38
NC_000003.11:g.30648372T>C , CM000665.1:g.30648372T>C	GRCh37
NC_000003.10:g.30623376T>C	NCBI36
NG_007490.1:g.5379T>C , LRG_779:g.5379T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.-4T>C MANE Select	ENSP00000295754.5:n.-4T>C
ENST00000295754.9:c.-4T>C	ENSP00000295754.5:n.-4T>C
ENST00000359013.4:c.-4T>C	ENSP00000351905.4:n.-4T>C
NM_001024847.2:c.-4T>C , LRG_779t1:c.-4T>C	NP_001020018.1:n.-4T>C
NM_003242.5:c.-4T>C	NP_003233.4:n.-4T>C
XM_011534045.1:c.-12+287T>C	XP_011532347.1:n.-12+287T>C
XM_011534045.3:c.-12+287T>C	XP_011532347.1:n.-12+287T>C
NM_003242.6:c.-4T>C MANE Select	NP_003233.4:n.-4T>C