Canonical Allele Identifier: CA2754892388
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875368C>T , CM000664.2:g.240875368C>T GRCh38
NC_000002.11:g.241814785C>T , CM000664.1:g.241814785C>T GRCh37
NC_000002.10:g.241463458C>T NCBI36
NG_008005.1:g.11624C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+164C>T MANE Select ENSP00000302620.3:n.776+164C>T
ENST00000307503.3:c.776+164C>T ENSP00000302620.3:n.776+164C>T
ENST00000476698.1:n.428+164C>T
NM_000030.2:c.776+164C>T NP_000021.1:n.776+164C>T
NM_000030.3:c.776+164C>T MANE Select NP_000021.1:n.776+164C>T
Search 100 bp 5'
Search 100 bp 3'