Canonical Allele Identifier: CA1339336348
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879206C= , CM000664.2:g.240879206C= GRCh38
NC_000002.11:g.241818623C= , CM000664.1:g.241818623C= GRCh37
NC_000002.10:g.241467296C= NCBI36
NG_008005.1:g.15462C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*385C= MANE Select ENSP00000302620.3:n.*385C=
ENST00000470255.1:n.1342C=
NM_000030.3:c.*385C= MANE Select NP_000021.1:n.*385C=
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