Canonical Allele Identifier: CA351316032
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240871419-C-A
MyVariant Identifiers: chr2:g.241810836C>A (hg19) chr2:g.240871419C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871419C>A , CM000664.2:g.240871419C>A GRCh38
NC_000002.11:g.241810836C>A , CM000664.1:g.241810836C>A GRCh37
NC_000002.10:g.241459509C>A NCBI36
NG_008005.1:g.7675C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.494C>A MANE Select ENSP00000302620.3:p.Pro165His
ENST00000307503.3:c.494C>A ENSP00000302620.3:p.Pro165His
ENST00000472436.1:n.514C>A
ENST00000476698.1:n.231C>A
NM_000030.2:c.494C>A NP_000021.1:p.Pro165His
NM_000030.3:c.494C>A MANE Select NP_000021.1:p.Pro165His
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