Canonical Allele Identifier: CA1339336342
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879195G= , CM000664.2:g.240879195G= GRCh38
NC_000002.11:g.241818612G= , CM000664.1:g.241818612G= GRCh37
NC_000002.10:g.241467285G= NCBI36
NG_008005.1:g.15451G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*374G= MANE Select ENSP00000302620.3:n.*374G=
ENST00000470255.1:n.1331G=
NM_000030.3:c.*374G= MANE Select NP_000021.1:n.*374G=