Canonical Allele Identifier: CA1339335715
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877981A= , CM000664.2:g.240877981A= GRCh38
NC_000002.11:g.241817398A= , CM000664.1:g.241817398A= GRCh37
NC_000002.10:g.241466071A= NCBI36
NG_008005.1:g.14237A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-41A= MANE Select ENSP00000302620.3:n.943-41A=
ENST00000307503.3:c.943-41A= ENSP00000302620.3:n.943-41A=
ENST00000470255.1:n.721-41A=
NM_000030.2:c.943-41A= NP_000021.1:n.943-41A=
NM_000030.3:c.943-41A= MANE Select NP_000021.1:n.943-41A=