Canonical Allele Identifier: CA1221528071

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345706G= , CM000663.2:g.218345706G=	GRCh38
NC_000001.10:g.218519048G= , CM000663.1:g.218519048G=	GRCh37
NC_000001.9:g.216585671G=	NCBI36
NG_027721.1:g.5373G=
NG_027721.2:g.5373G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-996G= MANE Select	ENSP00000355897.4:n.-996G=
NM_001135599.2:c.-996G=	NP_001129071.1:n.-996G=
NM_003238.3:c.-996G=	NP_003229.1:n.-996G=
NM_001135599.3:c.-996G=	NP_001129071.1:n.-996G=
NM_003238.4:c.-996G=	NP_003229.1:n.-996G=
NR_138148.1:n.423G=
NR_138149.1:n.423G=
NM_003238.5:c.-996G=	NP_003229.1:n.-996G=
NM_003238.6:c.-996G= MANE Select	NP_003229.1:n.-996G=
NM_001135599.4:c.-996G=	NP_001129071.1:n.-996G=
NR_138148.2:n.371G=
NR_138149.2:n.371G=