Canonical Allele Identifier: CA1339335433
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877419C= , CM000664.2:g.240877419C= GRCh38
NC_000002.11:g.241816836C= , CM000664.1:g.241816836C= GRCh37
NC_000002.10:g.241465509C= NCBI36
NG_008005.1:g.13675C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-118C= MANE Select ENSP00000302620.3:n.847-118C=
ENST00000307503.3:c.847-118C= ENSP00000302620.3:n.847-118C=
ENST00000470255.1:n.507C=
NM_000030.2:c.847-118C= NP_000021.1:n.847-118C=
NM_000030.3:c.847-118C= MANE Select NP_000021.1:n.847-118C=
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