Canonical Allele Identifier: CA432024435
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241814617A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875200A>C , CM000664.2:g.240875200A>C GRCh38
NC_000002.11:g.241814617A>C , CM000664.1:g.241814617A>C GRCh37
NC_000002.10:g.241463290A>C NCBI36
NG_008005.1:g.11456A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.772A>C MANE Select ENSP00000302620.3:p.Arg258=
ENST00000307503.3:c.772A>C ENSP00000302620.3:p.Arg258=
ENST00000476698.1:n.424A>C
NM_000030.2:c.772A>C NP_000021.1:p.Arg258=
NM_000030.3:c.772A>C MANE Select NP_000021.1:p.Arg258=
Search 100 bp 5'
Search 100 bp 3'