Canonical Allele Identifier: CA2697841541

Gene: TGFB2

Linked Data

• dbSNP Id: rs78975041

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437339A>C , CM000663.2:g.218437339A>C	GRCh38
NC_000001.10:g.218610681A>C , CM000663.1:g.218610681A>C	GRCh37
NC_000001.9:g.216677304A>C	NCBI36
NG_027721.1:g.97006A>C
NG_027721.2:g.97006A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.933-4A>C MANE Select	ENSP00000355897.4:n.933-4A>C
ENST00000366929.4:c.1017-4A>C	ENSP00000355896.4:n.1017-4A>C
ENST00000366930.8:c.933-4A>C	ENSP00000355897.4:n.933-4A>C
ENST00000479322.1:n.417-4A>C
NM_001135599.2:c.1017-4A>C	NP_001129071.1:n.1017-4A>C
NM_003238.3:c.933-4A>C	NP_003229.1:n.933-4A>C
NM_001135599.3:c.1017-4A>C	NP_001129071.1:n.1017-4A>C
NM_003238.4:c.933-4A>C	NP_003229.1:n.933-4A>C
NR_138148.1:n.2236-4A>C
NR_138149.1:n.2320-4A>C
NM_003238.5:c.933-4A>C	NP_003229.1:n.933-4A>C
NM_003238.6:c.933-4A>C MANE Select	NP_003229.1:n.933-4A>C
NM_001135599.4:c.1017-4A>C	NP_001129071.1:n.1017-4A>C
NR_138148.2:n.2184-4A>C
NR_138149.2:n.2268-4A>C