Canonical Allele Identifier: CA423176959

Gene: TGFB2 TGFB2-AS1

Linked Data

• dbSNP Id: rs2102525595
• MyVariant Identifiers: chr1:g.218518995G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345653G>A , CM000663.2:g.218345653G>A	GRCh38
NC_000001.10:g.218518995G>A , CM000663.1:g.218518995G>A	GRCh37
NC_000001.9:g.216585618G>A	NCBI36
NG_027721.1:g.5320G>A
NG_027721.2:g.5320G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1049G>A (TGFB2) MANE Select	ENSP00000355897.4:n.-1049G>A
NM_001135599.2:c.-1049G>A (TGFB2)	NP_001129071.1:n.-1049G>A
NM_003238.3:c.-1049G>A (TGFB2)	NP_003229.1:n.-1049G>A
NR_046268.1:n.26C>T (TGFB2-AS1)
NM_001135599.3:c.-1049G>A (TGFB2)	NP_001129071.1:n.-1049G>A
NM_003238.4:c.-1049G>A (TGFB2)	NP_003229.1:n.-1049G>A
NR_138148.1:n.370G>A (TGFB2)
NR_138149.1:n.370G>A (TGFB2)
NM_003238.5:c.-1049G>A (TGFB2)	NP_003229.1:n.-1049G>A
NM_003238.6:c.-1049G>A (TGFB2) MANE Select	NP_003229.1:n.-1049G>A
NM_001135599.4:c.-1049G>A (TGFB2)	NP_001129071.1:n.-1049G>A
NR_138148.2:n.318G>A (TGFB2)
NR_138149.2:n.318G>A (TGFB2)