Canonical Allele Identifier: CA423176883

Gene: TGFB2 TGFB2-AS1

Linked Data

• MyVariant Identifiers: chr1:g.218518969G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345627G>C , CM000663.2:g.218345627G>C	GRCh38
NC_000001.10:g.218518969G>C , CM000663.1:g.218518969G>C	GRCh37
NC_000001.9:g.216585592G>C	NCBI36
NG_027721.1:g.5294G>C
NG_027721.2:g.5294G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1075G>C (TGFB2) MANE Select	ENSP00000355897.4:n.-1075G>C
NM_001135599.2:c.-1075G>C (TGFB2)	NP_001129071.1:n.-1075G>C
NM_003238.3:c.-1075G>C (TGFB2)	NP_003229.1:n.-1075G>C
NR_046268.1:n.52C>G (TGFB2-AS1)
NM_001135599.3:c.-1075G>C (TGFB2)	NP_001129071.1:n.-1075G>C
NM_003238.4:c.-1075G>C (TGFB2)	NP_003229.1:n.-1075G>C
NR_138148.1:n.344G>C (TGFB2)
NR_138149.1:n.344G>C (TGFB2)
NM_003238.5:c.-1075G>C (TGFB2)	NP_003229.1:n.-1075G>C
NM_003238.6:c.-1075G>C (TGFB2) MANE Select	NP_003229.1:n.-1075G>C
NM_001135599.4:c.-1075G>C (TGFB2)	NP_001129071.1:n.-1075G>C
NR_138148.2:n.292G>C (TGFB2)
NR_138149.2:n.292G>C (TGFB2)