Canonical Allele Identifier: CA1339335500
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877541T= , CM000664.2:g.240877541T= GRCh38
NC_000002.11:g.241816958T= , CM000664.1:g.241816958T= GRCh37
NC_000002.10:g.241465631T= NCBI36
NG_008005.1:g.13797T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.851T= MANE Select ENSP00000302620.3:p.Leu284=
ENST00000307503.3:c.851T= ENSP00000302620.3:p.Leu284=
ENST00000470255.1:n.629T=
NM_000030.2:c.851T= NP_000021.1:p.Leu284=
NM_000030.3:c.851T= MANE Select NP_000021.1:p.Leu284=
Search 100 bp 5'
Search 100 bp 3'