Canonical Allele Identifier: CA2650531856

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218437284-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437284A>C , CM000663.2:g.218437284A>C	GRCh38
NC_000001.10:g.218610626A>C , CM000663.1:g.218610626A>C	GRCh37
NC_000001.9:g.216677249A>C	NCBI36
NG_027721.1:g.96951A>C
NG_027721.2:g.96951A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.933-59A>C MANE Select	ENSP00000355897.4:n.933-59A>C
ENST00000366929.4:c.1017-59A>C	ENSP00000355896.4:n.1017-59A>C
ENST00000366930.8:c.933-59A>C	ENSP00000355897.4:n.933-59A>C
ENST00000479322.1:n.417-59A>C
NM_001135599.2:c.1017-59A>C	NP_001129071.1:n.1017-59A>C
NM_003238.3:c.933-59A>C	NP_003229.1:n.933-59A>C
NM_001135599.3:c.1017-59A>C	NP_001129071.1:n.1017-59A>C
NM_003238.4:c.933-59A>C	NP_003229.1:n.933-59A>C
NR_138148.1:n.2236-59A>C
NR_138149.1:n.2320-59A>C
NM_003238.5:c.933-59A>C	NP_003229.1:n.933-59A>C
NM_003238.6:c.933-59A>C MANE Select	NP_003229.1:n.933-59A>C
NM_001135599.4:c.1017-59A>C	NP_001129071.1:n.1017-59A>C
NR_138148.2:n.2184-59A>C
NR_138149.2:n.2268-59A>C