Canonical Allele Identifier: CA1339336339
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879184T= , CM000664.2:g.240879184T= GRCh38
NC_000002.11:g.241818601T= , CM000664.1:g.241818601T= GRCh37
NC_000002.10:g.241467274T= NCBI36
NG_008005.1:g.15440T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*363T= MANE Select ENSP00000302620.3:n.*363T=
ENST00000470255.1:n.1320T=
NM_000030.3:c.*363T= MANE Select NP_000021.1:n.*363T=