Canonical Allele Identifier: CA1339336196
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878853C= , CM000664.2:g.240878853C= GRCh38
NC_000002.11:g.241818270C= , CM000664.1:g.241818270C= GRCh37
NC_000002.10:g.241466943C= NCBI36
NG_008005.1:g.15109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*32C= MANE Select ENSP00000302620.3:n.*32C=
ENST00000307503.3:c.*32C= ENSP00000302620.3:n.*32C=
ENST00000470255.1:n.989C=
NM_000030.2:c.*32C= NP_000021.1:n.*32C=
NM_000030.3:c.*32C= MANE Select NP_000021.1:n.*32C=