Canonical Allele Identifier: CA344725334
Gene: TGFB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.218520164C>A (hg19) chr1:g.218346822C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346822C>A , CM000663.2:g.218346822C>A GRCh38
NC_000001.10:g.218520164C>A , CM000663.1:g.218520164C>A GRCh37
NC_000001.9:g.216586787C>A NCBI36
NG_027721.1:g.6489C>A
NG_027721.2:g.6489C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.121C>A MANE Select ENSP00000355897.4:p.Arg41Ser
ENST00000366929.4:c.121C>A ENSP00000355896.4:p.Arg41Ser
ENST00000366930.8:c.121C>A ENSP00000355897.4:p.Arg41Ser
NM_001135599.2:c.121C>A NP_001129071.1:p.Arg41Ser
NM_003238.3:c.121C>A NP_003229.1:p.Arg41Ser
NM_001135599.3:c.121C>A NP_001129071.1:p.Arg41Ser
NM_003238.4:c.121C>A NP_003229.1:p.Arg41Ser
NR_138148.1:n.1539C>A
NR_138149.1:n.1539C>A
NM_003238.5:c.121C>A NP_003229.1:p.Arg41Ser
NM_003238.6:c.121C>A MANE Select NP_003229.1:p.Arg41Ser
NM_001135599.4:c.121C>A NP_001129071.1:p.Arg41Ser
NR_138148.2:n.1487C>A
NR_138149.2:n.1487C>A
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