Canonical Allele Identifier: CA423176904

Gene: TGFB2 TGFB2-AS1

Linked Data

• dbSNP Id: rs1558218777
• gnomAD v4: 1-218345634-C-T
• MyVariant Identifiers: chr1:g.218518976C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345634C>T , CM000663.2:g.218345634C>T	GRCh38
NC_000001.10:g.218518976C>T , CM000663.1:g.218518976C>T	GRCh37
NC_000001.9:g.216585599C>T	NCBI36
NG_027721.1:g.5301C>T
NG_027721.2:g.5301C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1068C>T (TGFB2) MANE Select	ENSP00000355897.4:n.-1068C>T
NM_001135599.2:c.-1068C>T (TGFB2)	NP_001129071.1:n.-1068C>T
NM_003238.3:c.-1068C>T (TGFB2)	NP_003229.1:n.-1068C>T
NR_046268.1:n.45G>A (TGFB2-AS1)
NM_001135599.3:c.-1068C>T (TGFB2)	NP_001129071.1:n.-1068C>T
NM_003238.4:c.-1068C>T (TGFB2)	NP_003229.1:n.-1068C>T
NR_138148.1:n.351C>T (TGFB2)
NR_138149.1:n.351C>T (TGFB2)
NM_003238.5:c.-1068C>T (TGFB2)	NP_003229.1:n.-1068C>T
NM_003238.6:c.-1068C>T (TGFB2) MANE Select	NP_003229.1:n.-1068C>T
NM_001135599.4:c.-1068C>T (TGFB2)	NP_001129071.1:n.-1068C>T
NR_138148.2:n.299C>T (TGFB2)
NR_138149.2:n.299C>T (TGFB2)