Canonical Allele Identifier: CA1221528595

Gene: TGFB2

Linked Data

• dbSNP Id: rs1656689588

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346673A>G , CM000663.2:g.218346673A>G	GRCh38
NC_000001.10:g.218520015A>G , CM000663.1:g.218520015A>G	GRCh37
NC_000001.9:g.216586638A>G	NCBI36
NG_027721.1:g.6340A>G
NG_027721.2:g.6340A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-29A>G MANE Select	ENSP00000355897.4:n.-29A>G
ENST00000366929.4:c.-29A>G	ENSP00000355896.4:n.-29A>G
ENST00000366930.8:c.-29A>G	ENSP00000355897.4:n.-29A>G
NM_001135599.2:c.-29A>G	NP_001129071.1:n.-29A>G
NM_003238.3:c.-29A>G	NP_003229.1:n.-29A>G
NM_001135599.3:c.-29A>G	NP_001129071.1:n.-29A>G
NM_003238.4:c.-29A>G	NP_003229.1:n.-29A>G
NR_138148.1:n.1390A>G
NR_138149.1:n.1390A>G
NM_003238.5:c.-29A>G	NP_003229.1:n.-29A>G
NM_003238.6:c.-29A>G MANE Select	NP_003229.1:n.-29A>G
NM_001135599.4:c.-29A>G	NP_001129071.1:n.-29A>G
NR_138148.2:n.1338A>G
NR_138149.2:n.1338A>G