Canonical Allele Identifier: CA1339336065
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878593C= , CM000664.2:g.240878593C= GRCh38
NC_000002.11:g.241818010C= , CM000664.1:g.241818010C= GRCh37
NC_000002.10:g.241466683C= NCBI36
NG_008005.1:g.14849C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-121C= MANE Select ENSP00000302620.3:n.1072-121C=
ENST00000307503.3:c.1072-121C= ENSP00000302620.3:n.1072-121C=
ENST00000470255.1:n.850-121C=
NM_000030.2:c.1072-121C= NP_000021.1:n.1072-121C=
NM_000030.3:c.1072-121C= MANE Select NP_000021.1:n.1072-121C=