Canonical Allele Identifier: CA2664010855
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877363C>A , CM000664.2:g.240877363C>A GRCh38
NC_000002.11:g.241816780C>A , CM000664.1:g.241816780C>A GRCh37
NC_000002.10:g.241465453C>A NCBI36
NG_008005.1:g.13619C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-174C>A MANE Select ENSP00000302620.3:n.847-174C>A
ENST00000307503.3:c.847-174C>A ENSP00000302620.3:n.847-174C>A
ENST00000470255.1:n.451C>A
NM_000030.2:c.847-174C>A NP_000021.1:n.847-174C>A
NM_000030.3:c.847-174C>A MANE Select NP_000021.1:n.847-174C>A