Canonical Allele Identifier: CA1339336038
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878515G= , CM000664.2:g.240878515G= GRCh38
NC_000002.11:g.241817932G= , CM000664.1:g.241817932G= GRCh37
NC_000002.10:g.241466605G= NCBI36
NG_008005.1:g.14771G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-199G= MANE Select ENSP00000302620.3:n.1072-199G=
ENST00000307503.3:c.1072-199G= ENSP00000302620.3:n.1072-199G=
ENST00000470255.1:n.850-199G=
NM_000030.2:c.1072-199G= NP_000021.1:n.1072-199G=
NM_000030.3:c.1072-199G= MANE Select NP_000021.1:n.1072-199G=