Canonical Allele Identifier: CA1221566072

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437363G= , CM000663.2:g.218437363G=	GRCh38
NC_000001.10:g.218610705G= , CM000663.1:g.218610705G=	GRCh37
NC_000001.9:g.216677328G=	NCBI36
NG_027721.1:g.97030G=
NG_027721.2:g.97030G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003238.6:c.953G= MANE Select	NP_003229.1:p.Cys318=
ENST00000366930.9:c.953G= MANE Select	ENSP00000355897.4:p.Cys318=
NM_001135599.2:c.1037G=	NP_001129071.1:p.Cys346=
NM_001135599.3:c.1037G=	NP_001129071.1:p.Cys346=
NM_001135599.4:c.1037G=	NP_001129071.1:p.Cys346=
NM_003238.3:c.953G=	NP_003229.1:p.Cys318=
NM_003238.4:c.953G=	NP_003229.1:p.Cys318=
NM_003238.5:c.953G=	NP_003229.1:p.Cys318=
NR_138148.1:n.2256G=
NR_138148.2:n.2204G=
NR_138149.1:n.2340G=
NR_138149.2:n.2288G=
ENST00000366929.4:c.1037G=	ENSP00000355896.4:p.Cys346=
ENST00000366930.8:c.953G=	ENSP00000355897.4:p.Cys318=
ENST00000479322.1:n.437G=