Canonical Allele Identifier: CA344725318

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218520157G>C (hg19) ; chr1:g.218346815G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346815G>C , CM000663.2:g.218346815G>C	GRCh38
NC_000001.10:g.218520157G>C , CM000663.1:g.218520157G>C	GRCh37
NC_000001.9:g.216586780G>C	NCBI36
NG_027721.1:g.6482G>C
NG_027721.2:g.6482G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.114G>C MANE Select	ENSP00000355897.4:p.Glu38Asp
ENST00000366929.4:c.114G>C	ENSP00000355896.4:p.Glu38Asp
ENST00000366930.8:c.114G>C	ENSP00000355897.4:p.Glu38Asp
NM_001135599.2:c.114G>C	NP_001129071.1:p.Glu38Asp
NM_003238.3:c.114G>C	NP_003229.1:p.Glu38Asp
NM_001135599.3:c.114G>C	NP_001129071.1:p.Glu38Asp
NM_003238.4:c.114G>C	NP_003229.1:p.Glu38Asp
NR_138148.1:n.1532G>C
NR_138149.1:n.1532G>C
NM_003238.5:c.114G>C	NP_003229.1:p.Glu38Asp
NM_003238.6:c.114G>C MANE Select	NP_003229.1:p.Glu38Asp
NM_001135599.4:c.114G>C	NP_001129071.1:p.Glu38Asp
NR_138148.2:n.1480G>C
NR_138149.2:n.1480G>C