Canonical Allele Identifier: CA1339336315
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879118C= , CM000664.2:g.240879118C= GRCh38
NC_000002.11:g.241818535C= , CM000664.1:g.241818535C= GRCh37
NC_000002.10:g.241467208C= NCBI36
NG_008005.1:g.15374C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*297C= MANE Select ENSP00000302620.3:n.*297C=
ENST00000307503.3:c.*297C= ENSP00000302620.3:n.*297C=
ENST00000470255.1:n.1254C=
NM_000030.2:c.*297C= NP_000021.1:n.*297C=
NM_000030.3:c.*297C= MANE Select NP_000021.1:n.*297C=