Canonical Allele Identifier: CA2664006125
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869395G>A , CM000664.2:g.240869395G>A GRCh38
NC_000002.11:g.241808812G>A , CM000664.1:g.241808812G>A GRCh37
NC_000002.10:g.241457485G>A NCBI36
NG_008005.1:g.5651G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+33G>A MANE Select ENSP00000302620.3:n.358+33G>A
ENST00000307503.3:c.358+33G>A ENSP00000302620.3:n.358+33G>A
ENST00000472436.1:n.378+33G>A
NM_000030.2:c.358+33G>A NP_000021.1:n.358+33G>A
XR_924060.1:n.405+838C>T
NM_000030.3:c.358+33G>A MANE Select NP_000021.1:n.358+33G>A