Canonical Allele Identifier: CA1339333592
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240874045C= , CM000664.2:g.240874045C= GRCh38
NC_000002.11:g.241813462C= , CM000664.1:g.241813462C= GRCh37
NC_000002.10:g.241462135C= NCBI36
NG_008005.1:g.10301C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.663C= MANE Select ENSP00000302620.3:p.Ser221=
ENST00000307503.3:c.663C= ENSP00000302620.3:p.Ser221=
ENST00000476698.1:n.332+996C=
NM_000030.2:c.663C= NP_000021.1:p.Ser221=
NM_000030.3:c.663C= MANE Select NP_000021.1:p.Ser221=