Canonical Allele Identifier: CA731608417

Gene: TGFB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218436360A>T , CM000663.2:g.218436360A>T	GRCh38
NC_000001.10:g.218609702A>T , CM000663.1:g.218609702A>T	GRCh37
NC_000001.9:g.216676325A>T	NCBI36
NG_027721.1:g.96027A>T
NG_027721.2:g.96027A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.932+213A>T MANE Select	ENSP00000355897.4:n.932+213A>T
ENST00000366929.4:c.1016+213A>T	ENSP00000355896.4:n.1016+213A>T
ENST00000366930.8:c.932+213A>T	ENSP00000355897.4:n.932+213A>T
ENST00000479322.1:n.416+213A>T
NM_001135599.2:c.1016+213A>T	NP_001129071.1:n.1016+213A>T
NM_003238.3:c.932+213A>T	NP_003229.1:n.932+213A>T
NM_001135599.3:c.1016+213A>T	NP_001129071.1:n.1016+213A>T
NM_003238.4:c.932+213A>T	NP_003229.1:n.932+213A>T
NR_138148.1:n.2235+213A>T
NR_138149.1:n.2319+213A>T
NM_003238.5:c.932+213A>T	NP_003229.1:n.932+213A>T
NM_003238.6:c.932+213A>T MANE Select	NP_003229.1:n.932+213A>T
NM_001135599.4:c.1016+213A>T	NP_001129071.1:n.1016+213A>T
NR_138148.2:n.2183+213A>T
NR_138149.2:n.2267+213A>T