Canonical Allele Identifier: CA423176876
Gene: TGFB2 HGNC NCBI
TGFB2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.218518967G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345625G>A , CM000663.2:g.218345625G>A GRCh38
NC_000001.10:g.218518967G>A , CM000663.1:g.218518967G>A GRCh37
NC_000001.9:g.216585590G>A NCBI36
NG_027721.1:g.5292G>A
NG_027721.2:g.5292G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-1077G>A (TGFB2) MANE Select ENSP00000355897.4:n.-1077G>A
NM_001135599.2:c.-1077G>A (TGFB2) NP_001129071.1:n.-1077G>A
NM_003238.3:c.-1077G>A (TGFB2) NP_003229.1:n.-1077G>A
NR_046268.1:n.54C>T (TGFB2-AS1)
NM_001135599.3:c.-1077G>A (TGFB2) NP_001129071.1:n.-1077G>A
NM_003238.4:c.-1077G>A (TGFB2) NP_003229.1:n.-1077G>A
NR_138148.1:n.342G>A (TGFB2)
NR_138149.1:n.342G>A (TGFB2)
NM_003238.5:c.-1077G>A (TGFB2) NP_003229.1:n.-1077G>A
NM_003238.6:c.-1077G>A (TGFB2) MANE Select NP_003229.1:n.-1077G>A
NM_001135599.4:c.-1077G>A (TGFB2) NP_001129071.1:n.-1077G>A
NR_138148.2:n.290G>A (TGFB2)
NR_138149.2:n.290G>A (TGFB2)