Canonical Allele Identifier: CA1221566213

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437437G= , CM000663.2:g.218437437G=	GRCh38
NC_000001.10:g.218610779G= , CM000663.1:g.218610779G=	GRCh37
NC_000001.9:g.216677402G=	NCBI36
NG_027721.1:g.97104G=
NG_027721.2:g.97104G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1027G= MANE Select	ENSP00000355897.4:p.Ala343=
ENST00000366929.4:c.1111G=	ENSP00000355896.4:p.Ala371=
ENST00000366930.8:c.1027G=	ENSP00000355897.4:p.Ala343=
ENST00000479322.1:n.511G=
NM_001135599.2:c.1111G=	NP_001129071.1:p.Ala371=
NM_003238.3:c.1027G=	NP_003229.1:p.Ala343=
NM_001135599.3:c.1111G=	NP_001129071.1:p.Ala371=
NM_003238.4:c.1027G=	NP_003229.1:p.Ala343=
NR_138148.1:n.2330G=
NR_138149.1:n.2414G=
NM_003238.5:c.1027G=	NP_003229.1:p.Ala343=
NM_003238.6:c.1027G= MANE Select	NP_003229.1:p.Ala343=
NM_001135599.4:c.1111G=	NP_001129071.1:p.Ala371=
NR_138148.2:n.2278G=
NR_138149.2:n.2362G=