Canonical Allele Identifier: CA2754892481
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879059C>G , CM000664.2:g.240879059C>G GRCh38
NC_000002.11:g.241818476C>G , CM000664.1:g.241818476C>G GRCh37
NC_000002.10:g.241467149C>G NCBI36
NG_008005.1:g.15315C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*238C>G MANE Select ENSP00000302620.3:n.*238C>G
ENST00000307503.3:c.*238C>G ENSP00000302620.3:n.*238C>G
ENST00000470255.1:n.1195C>G
NM_000030.2:c.*238C>G NP_000021.1:n.*238C>G
NM_000030.3:c.*238C>G MANE Select NP_000021.1:n.*238C>G