Canonical Allele Identifier: CA1339336078
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878627A= , CM000664.2:g.240878627A= GRCh38
NC_000002.11:g.241818044A= , CM000664.1:g.241818044A= GRCh37
NC_000002.10:g.241466717A= NCBI36
NG_008005.1:g.14883A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-87A= MANE Select ENSP00000302620.3:n.1072-87A=
ENST00000307503.3:c.1072-87A= ENSP00000302620.3:n.1072-87A=
ENST00000470255.1:n.850-87A=
NM_000030.2:c.1072-87A= NP_000021.1:n.1072-87A=
NM_000030.3:c.1072-87A= MANE Select NP_000021.1:n.1072-87A=