Canonical Allele Identifier: CA1012386628

Gene: TGFB2

Linked Data

• dbSNP Id: rs78166872
• gnomAD v3: 1-218437338-A-T
• gnomAD v4: 1-218437338-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437338A>T , CM000663.2:g.218437338A>T	GRCh38
NC_000001.10:g.218610680A>T , CM000663.1:g.218610680A>T	GRCh37
NC_000001.9:g.216677303A>T	NCBI36
NG_027721.1:g.97005A>T
NG_027721.2:g.97005A>T

Transcript Alleles

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