Canonical Allele Identifier: CA2577302758
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877988C>T , CM000664.2:g.240877988C>T GRCh38
NC_000002.11:g.241817405C>T , CM000664.1:g.241817405C>T GRCh37
NC_000002.10:g.241466078C>T NCBI36
NG_008005.1:g.14244C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.943-34C>T MANE Select ENSP00000302620.3:n.943-34C>T
ENST00000307503.3:c.943-34C>T ENSP00000302620.3:n.943-34C>T
ENST00000470255.1:n.721-34C>T
NM_000030.2:c.943-34C>T NP_000021.1:n.943-34C>T
NM_000030.3:c.943-34C>T MANE Select NP_000021.1:n.943-34C>T
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