Canonical Allele Identifier: CA423176956

Gene: TGFB2 TGFB2-AS1

Linked Data

• dbSNP Id: rs1373610611
• gnomAD v3: 1-218345652-G-T
• gnomAD v4: 1-218345652-G-T
• MyVariant Identifiers: chr1:g.218518994G>T (hg19) ; chr1:g.218345652G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345652G>T , CM000663.2:g.218345652G>T	GRCh38
NC_000001.10:g.218518994G>T , CM000663.1:g.218518994G>T	GRCh37
NC_000001.9:g.216585617G>T	NCBI36
NG_027721.1:g.5319G>T
NG_027721.2:g.5319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1050G>T (TGFB2) MANE Select	ENSP00000355897.4:n.-1050G>T
NM_001135599.2:c.-1050G>T (TGFB2)	NP_001129071.1:n.-1050G>T
NM_003238.3:c.-1050G>T (TGFB2)	NP_003229.1:n.-1050G>T
NR_046268.1:n.27C>A (TGFB2-AS1)
NM_001135599.3:c.-1050G>T (TGFB2)	NP_001129071.1:n.-1050G>T
NM_003238.4:c.-1050G>T (TGFB2)	NP_003229.1:n.-1050G>T
NR_138148.1:n.369G>T (TGFB2)
NR_138149.1:n.369G>T (TGFB2)
NM_003238.5:c.-1050G>T (TGFB2)	NP_003229.1:n.-1050G>T
NM_003238.6:c.-1050G>T (TGFB2) MANE Select	NP_003229.1:n.-1050G>T
NM_001135599.4:c.-1050G>T (TGFB2)	NP_001129071.1:n.-1050G>T
NR_138148.2:n.317G>T (TGFB2)
NR_138149.2:n.317G>T (TGFB2)