Canonical Allele Identifier: CA344726573
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218434154G>C , CM000663.2:g.218434154G>C GRCh38
NC_000001.10:g.218607496G>C , CM000663.1:g.218607496G>C GRCh37
NC_000001.9:g.216674119G>C NCBI36
NG_027721.1:g.93821G>C
NG_027721.2:g.93821G>C

Transcript Alleles

HGVS Amino-acid Change
NM_003238.6:c.583G>C MANE Select NP_003229.1:p.Glu195Gln
ENST00000366930.9:c.583G>C MANE Select ENSP00000355897.4:p.Glu195Gln
NM_001135599.2:c.667G>C NP_001129071.1:p.Glu223Gln
NM_001135599.3:c.667G>C NP_001129071.1:p.Glu223Gln
NM_001135599.4:c.667G>C NP_001129071.1:p.Glu223Gln
NM_003238.3:c.583G>C NP_003229.1:p.Glu195Gln
NM_003238.4:c.583G>C NP_003229.1:p.Glu195Gln
NM_003238.5:c.583G>C NP_003229.1:p.Glu195Gln
NR_138148.1:n.2001G>C
NR_138148.2:n.1949G>C
NR_138149.1:n.2085G>C
NR_138149.2:n.2033G>C
ENST00000366929.4:c.667G>C ENSP00000355896.4:p.Glu223Gln
ENST00000366930.8:c.583G>C ENSP00000355897.4:p.Glu195Gln
ENST00000479322.1:n.29G>C
ENST00000488793.1:n.247G>C