Canonical Allele Identifier: CA351319347
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241817036T>A (hg19) chr2:g.240877619T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877619T>A , CM000664.2:g.240877619T>A GRCh38
NC_000002.11:g.241817036T>A , CM000664.1:g.241817036T>A GRCh37
NC_000002.10:g.241465709T>A NCBI36
NG_008005.1:g.13875T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.929T>A MANE Select ENSP00000302620.3:p.Phe310Tyr
ENST00000307503.3:c.929T>A ENSP00000302620.3:p.Phe310Tyr
ENST00000470255.1:n.707T>A
NM_000030.2:c.929T>A NP_000021.1:p.Phe310Tyr
NM_000030.3:c.929T>A MANE Select NP_000021.1:p.Phe310Tyr
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