Canonical Allele Identifier: CA37625733

Gene: TGFB2

Linked Data

• dbSNP Id: rs772714576
• gnomAD v3: 1-218441419-G-A
• gnomAD v4: 1-218441419-G-A
• MyVariant Identifiers: chr1:g.218614761G>A (hg19) ; chr1:g.218441419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441419G>A , CM000663.2:g.218441419G>A	GRCh38
NC_000001.10:g.218614761G>A , CM000663.1:g.218614761G>A	GRCh37
NC_000001.9:g.216681384G>A	NCBI36
NG_027721.1:g.101086G>A
NG_027721.2:g.101086G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*57G>A MANE Select	ENSP00000355897.4:n.*57G>A
ENST00000366929.4:c.*57G>A	ENSP00000355896.4:n.*57G>A
ENST00000366930.8:c.*57G>A	ENSP00000355897.4:n.*57G>A
ENST00000479322.1:n.786G>A
NM_001135599.2:c.*57G>A	NP_001129071.1:n.*57G>A
NM_003238.3:c.*57G>A	NP_003229.1:n.*57G>A
NM_001135599.3:c.*57G>A	NP_001129071.1:n.*57G>A
NM_003238.4:c.*57G>A	NP_003229.1:n.*57G>A
NR_138148.1:n.2605G>A
NR_138149.1:n.2689G>A
NM_003238.5:c.*57G>A	NP_003229.1:n.*57G>A
NM_003238.6:c.*57G>A MANE Select	NP_003229.1:n.*57G>A
NM_001135599.4:c.*57G>A	NP_001129071.1:n.*57G>A
NR_138148.2:n.2553G>A
NR_138149.2:n.2637G>A