Canonical Allele Identifier: CA2209069
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs755578184

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869402C>A , CM000664.2:g.240869402C>A GRCh38
NC_000002.11:g.241808819C>A , CM000664.1:g.241808819C>A GRCh37
NC_000002.10:g.241457492C>A NCBI36
NG_008005.1:g.5658C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+40C>A MANE Select ENSP00000302620.3:n.358+40C>A
ENST00000307503.3:c.358+40C>A ENSP00000302620.3:n.358+40C>A
ENST00000472436.1:n.378+40C>A
NM_000030.2:c.358+40C>A NP_000021.1:n.358+40C>A
XR_924060.1:n.405+831G>T
NM_000030.3:c.358+40C>A MANE Select NP_000021.1:n.358+40C>A