Canonical Allele Identifier: CA351319189
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877577C>G , CM000664.2:g.240877577C>G GRCh38
NC_000002.11:g.241816994C>G , CM000664.1:g.241816994C>G GRCh37
NC_000002.10:g.241465667C>G NCBI36
NG_008005.1:g.13833C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.887C>G MANE Select ENSP00000302620.3:p.Ala296Gly
ENST00000307503.3:c.887C>G ENSP00000302620.3:p.Ala296Gly
ENST00000470255.1:n.665C>G
NM_000030.2:c.887C>G NP_000021.1:p.Ala296Gly
NM_000030.3:c.887C>G MANE Select NP_000021.1:p.Ala296Gly