Canonical Allele Identifier: CA1221565860

Gene: TGFB2

Linked Data

• dbSNP Id: rs1659998055

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437213T>C , CM000663.2:g.218437213T>C	GRCh38
NC_000001.10:g.218610555T>C , CM000663.1:g.218610555T>C	GRCh37
NC_000001.9:g.216677178T>C	NCBI36
NG_027721.1:g.96880T>C
NG_027721.2:g.96880T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.933-130T>C MANE Select	ENSP00000355897.4:n.933-130T>C
ENST00000366929.4:c.1017-130T>C	ENSP00000355896.4:n.1017-130T>C
ENST00000366930.8:c.933-130T>C	ENSP00000355897.4:n.933-130T>C
ENST00000479322.1:n.417-130T>C
NM_001135599.2:c.1017-130T>C	NP_001129071.1:n.1017-130T>C
NM_003238.3:c.933-130T>C	NP_003229.1:n.933-130T>C
NM_001135599.3:c.1017-130T>C	NP_001129071.1:n.1017-130T>C
NM_003238.4:c.933-130T>C	NP_003229.1:n.933-130T>C
NR_138148.1:n.2236-130T>C
NR_138149.1:n.2320-130T>C
NM_003238.5:c.933-130T>C	NP_003229.1:n.933-130T>C
NM_003238.6:c.933-130T>C MANE Select	NP_003229.1:n.933-130T>C
NM_001135599.4:c.1017-130T>C	NP_001129071.1:n.1017-130T>C
NR_138148.2:n.2184-130T>C
NR_138149.2:n.2268-130T>C