Canonical Allele Identifier: CA1339336330
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879162T= , CM000664.2:g.240879162T= GRCh38
NC_000002.11:g.241818579T= , CM000664.1:g.241818579T= GRCh37
NC_000002.10:g.241467252T= NCBI36
NG_008005.1:g.15418T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*341T= MANE Select ENSP00000302620.3:n.*341T=
ENST00000470255.1:n.1298T=
NM_000030.3:c.*341T= MANE Select NP_000021.1:n.*341T=