Canonical Allele Identifier: CA2698019368

Gene: TGFB2

Linked Data

• dbSNP Id: rs2102527966

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218347057T>C , CM000663.2:g.218347057T>C	GRCh38
NC_000001.10:g.218520399T>C , CM000663.1:g.218520399T>C	GRCh37
NC_000001.9:g.216587022T>C	NCBI36
NG_027721.1:g.6724T>C
NG_027721.2:g.6724T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.346+10T>C MANE Select	ENSP00000355897.4:n.346+10T>C
ENST00000366929.4:c.346+10T>C	ENSP00000355896.4:n.346+10T>C
ENST00000366930.8:c.346+10T>C	ENSP00000355897.4:n.346+10T>C
ENST00000488793.1:n.10+10T>C
NM_001135599.2:c.346+10T>C	NP_001129071.1:n.346+10T>C
NM_003238.3:c.346+10T>C	NP_003229.1:n.346+10T>C
NM_001135599.3:c.346+10T>C	NP_001129071.1:n.346+10T>C
NM_003238.4:c.346+10T>C	NP_003229.1:n.346+10T>C
NR_138148.1:n.1764+10T>C
NR_138149.1:n.1764+10T>C
NM_003238.5:c.346+10T>C	NP_003229.1:n.346+10T>C
NM_003238.6:c.346+10T>C MANE Select	NP_003229.1:n.346+10T>C
NM_001135599.4:c.346+10T>C	NP_001129071.1:n.346+10T>C
NR_138148.2:n.1712+10T>C
NR_138149.2:n.1712+10T>C