Canonical Allele Identifier: CA1339335465
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877479C= , CM000664.2:g.240877479C= GRCh38
NC_000002.11:g.241816896C= , CM000664.1:g.241816896C= GRCh37
NC_000002.10:g.241465569C= NCBI36
NG_008005.1:g.13735C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.847-58C= MANE Select ENSP00000302620.3:n.847-58C=
ENST00000307503.3:c.847-58C= ENSP00000302620.3:n.847-58C=
ENST00000470255.1:n.567C=
NM_000030.2:c.847-58C= NP_000021.1:n.847-58C=
NM_000030.3:c.847-58C= MANE Select NP_000021.1:n.847-58C=