Canonical Allele Identifier: CA2650531273

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218346675-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346675C>A , CM000663.2:g.218346675C>A	GRCh38
NC_000001.10:g.218520017C>A , CM000663.1:g.218520017C>A	GRCh37
NC_000001.9:g.216586640C>A	NCBI36
NG_027721.1:g.6342C>A
NG_027721.2:g.6342C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-27C>A MANE Select	ENSP00000355897.4:n.-27C>A
ENST00000366929.4:c.-27C>A	ENSP00000355896.4:n.-27C>A
ENST00000366930.8:c.-27C>A	ENSP00000355897.4:n.-27C>A
NM_001135599.2:c.-27C>A	NP_001129071.1:n.-27C>A
NM_003238.3:c.-27C>A	NP_003229.1:n.-27C>A
NM_001135599.3:c.-27C>A	NP_001129071.1:n.-27C>A
NM_003238.4:c.-27C>A	NP_003229.1:n.-27C>A
NR_138148.1:n.1392C>A
NR_138149.1:n.1392C>A
NM_003238.5:c.-27C>A	NP_003229.1:n.-27C>A
NM_003238.6:c.-27C>A MANE Select	NP_003229.1:n.-27C>A
NM_001135599.4:c.-27C>A	NP_001129071.1:n.-27C>A
NR_138148.2:n.1340C>A
NR_138149.2:n.1340C>A