Canonical Allele Identifier: CA915944003

Gene: TGFB2

Linked Data

• ClinVar Variation Id: 681541
• ClinVar RCV Id: RCV000841468
• dbSNP Id: rs1571820524

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346698A>C , CM000663.2:g.218346698A>C	GRCh38
NC_000001.10:g.218520040A>C , CM000663.1:g.218520040A>C	GRCh37
NC_000001.9:g.216586663A>C	NCBI36
NG_027721.1:g.6365A>C
NG_027721.2:g.6365A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-4A>C MANE Select	ENSP00000355897.4:n.-4A>C
ENST00000366929.4:c.-4A>C	ENSP00000355896.4:n.-4A>C
ENST00000366930.8:c.-4A>C	ENSP00000355897.4:n.-4A>C
NM_001135599.2:c.-4A>C	NP_001129071.1:n.-4A>C
NM_003238.3:c.-4A>C	NP_003229.1:n.-4A>C
NM_001135599.3:c.-4A>C	NP_001129071.1:n.-4A>C
NM_003238.4:c.-4A>C	NP_003229.1:n.-4A>C
NR_138148.1:n.1415A>C
NR_138149.1:n.1415A>C
NM_003238.5:c.-4A>C	NP_003229.1:n.-4A>C
NM_003238.6:c.-4A>C MANE Select	NP_003229.1:n.-4A>C
NM_001135599.4:c.-4A>C	NP_001129071.1:n.-4A>C
NR_138148.2:n.1363A>C
NR_138149.2:n.1363A>C