Canonical Allele Identifier: CA344725385
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346846A>C , CM000663.2:g.218346846A>C GRCh38
NC_000001.10:g.218520188A>C , CM000663.1:g.218520188A>C GRCh37
NC_000001.9:g.216586811A>C NCBI36
NG_027721.1:g.6513A>C
NG_027721.2:g.6513A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.145A>C MANE Select ENSP00000355897.4:p.Lys49Gln
ENST00000366929.4:c.145A>C ENSP00000355896.4:p.Lys49Gln
ENST00000366930.8:c.145A>C ENSP00000355897.4:p.Lys49Gln
NM_001135599.2:c.145A>C NP_001129071.1:p.Lys49Gln
NM_003238.3:c.145A>C NP_003229.1:p.Lys49Gln
NM_001135599.3:c.145A>C NP_001129071.1:p.Lys49Gln
NM_003238.4:c.145A>C NP_003229.1:p.Lys49Gln
NR_138148.1:n.1563A>C
NR_138149.1:n.1563A>C
NM_003238.5:c.145A>C NP_003229.1:p.Lys49Gln
NM_003238.6:c.145A>C MANE Select NP_003229.1:p.Lys49Gln
NM_001135599.4:c.145A>C NP_001129071.1:p.Lys49Gln
NR_138148.2:n.1511A>C
NR_138149.2:n.1511A>C