Canonical Allele Identifier: CA351319717
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878713G>A , CM000664.2:g.240878713G>A GRCh38
NC_000002.11:g.241818130G>A , CM000664.1:g.241818130G>A GRCh37
NC_000002.10:g.241466803G>A NCBI36
NG_008005.1:g.14969G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-1G>A MANE Select ENSP00000302620.3:n.1072-1G>A
ENST00000307503.3:c.1072-1G>A ENSP00000302620.3:n.1072-1G>A
ENST00000470255.1:n.850-1G>A
NM_000030.2:c.1072-1G>A NP_000021.1:n.1072-1G>A
NM_000030.3:c.1072-1G>A MANE Select NP_000021.1:n.1072-1G>A