Canonical Allele Identifier: CA1339333036
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240872931G= , CM000664.2:g.240872931G= GRCh38
NC_000002.11:g.241812348G= , CM000664.1:g.241812348G= GRCh37
NC_000002.10:g.241461021G= NCBI36
NG_008005.1:g.9187G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.525-48G= MANE Select ENSP00000302620.3:n.525-48G=
ENST00000307503.3:c.525-48G= ENSP00000302620.3:n.525-48G=
ENST00000472436.1:n.545-48G=
ENST00000476698.1:n.262-48G=
NM_000030.2:c.525-48G= NP_000021.1:n.525-48G=
NM_000030.3:c.525-48G= MANE Select NP_000021.1:n.525-48G=
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