Canonical Allele Identifier: CA423176850

Gene: TGFB2 TGFB2-AS1

Linked Data

• gnomAD v4: 1-218345616-T-C
• MyVariant Identifiers: chr1:g.218518958T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345616T>C , CM000663.2:g.218345616T>C	GRCh38
NC_000001.10:g.218518958T>C , CM000663.1:g.218518958T>C	GRCh37
NC_000001.9:g.216585581T>C	NCBI36
NG_027721.1:g.5283T>C
NG_027721.2:g.5283T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1086T>C (TGFB2) MANE Select	ENSP00000355897.4:n.-1086T>C
NM_001135599.2:c.-1086T>C (TGFB2)	NP_001129071.1:n.-1086T>C
NM_003238.3:c.-1086T>C (TGFB2)	NP_003229.1:n.-1086T>C
NR_046268.1:n.63A>G (TGFB2-AS1)
NM_001135599.3:c.-1086T>C (TGFB2)	NP_001129071.1:n.-1086T>C
NM_003238.4:c.-1086T>C (TGFB2)	NP_003229.1:n.-1086T>C
NR_138148.1:n.333T>C (TGFB2)
NR_138149.1:n.333T>C (TGFB2)
NM_003238.5:c.-1086T>C (TGFB2)	NP_003229.1:n.-1086T>C
NM_003238.6:c.-1086T>C (TGFB2) MANE Select	NP_003229.1:n.-1086T>C
NM_001135599.4:c.-1086T>C (TGFB2)	NP_001129071.1:n.-1086T>C
NR_138148.2:n.281T>C (TGFB2)
NR_138149.2:n.281T>C (TGFB2)