Canonical Allele Identifier: CA2607207532

Gene: TGFB2

Linked Data

• dbSNP Id: rs2102634709
• gnomAD v3: 1-218441425-A-C
• gnomAD v4: 1-218441425-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441425A>C , CM000663.2:g.218441425A>C	GRCh38
NC_000001.10:g.218614767A>C , CM000663.1:g.218614767A>C	GRCh37
NC_000001.9:g.216681390A>C	NCBI36
NG_027721.1:g.101092A>C
NG_027721.2:g.101092A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*63A>C MANE Select	ENSP00000355897.4:n.*63A>C
ENST00000366929.4:c.*63A>C	ENSP00000355896.4:n.*63A>C
ENST00000366930.8:c.*63A>C	ENSP00000355897.4:n.*63A>C
ENST00000479322.1:n.792A>C
NM_001135599.2:c.*63A>C	NP_001129071.1:n.*63A>C
NM_003238.3:c.*63A>C	NP_003229.1:n.*63A>C
NM_001135599.3:c.*63A>C	NP_001129071.1:n.*63A>C
NM_003238.4:c.*63A>C	NP_003229.1:n.*63A>C
NR_138148.1:n.2611A>C
NR_138149.1:n.2695A>C
NM_003238.5:c.*63A>C	NP_003229.1:n.*63A>C
NM_003238.6:c.*63A>C MANE Select	NP_003229.1:n.*63A>C
NM_001135599.4:c.*63A>C	NP_001129071.1:n.*63A>C
NR_138148.2:n.2559A>C
NR_138149.2:n.2643A>C