Canonical Allele Identifier: CA423173669

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218610772G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437430G>C , CM000663.2:g.218437430G>C	GRCh38
NC_000001.10:g.218610772G>C , CM000663.1:g.218610772G>C	GRCh37
NC_000001.9:g.216677395G>C	NCBI36
NG_027721.1:g.97097G>C
NG_027721.2:g.97097G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.1020G>C MANE Select	ENSP00000355897.4:p.Gly340=
ENST00000366929.4:c.1104G>C	ENSP00000355896.4:p.Gly368=
ENST00000366930.8:c.1020G>C	ENSP00000355897.4:p.Gly340=
ENST00000479322.1:n.504G>C
NM_001135599.2:c.1104G>C	NP_001129071.1:p.Gly368=
NM_003238.3:c.1020G>C	NP_003229.1:p.Gly340=
NM_001135599.3:c.1104G>C	NP_001129071.1:p.Gly368=
NM_003238.4:c.1020G>C	NP_003229.1:p.Gly340=
NR_138148.1:n.2323G>C
NR_138149.1:n.2407G>C
NM_003238.5:c.1020G>C	NP_003229.1:p.Gly340=
NM_003238.6:c.1020G>C MANE Select	NP_003229.1:p.Gly340=
NM_001135599.4:c.1104G>C	NP_001129071.1:p.Gly368=
NR_138148.2:n.2271G>C
NR_138149.2:n.2355G>C