Canonical Allele Identifier: CA766960554
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1252949313

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869106G>A , CM000664.2:g.240869106G>A GRCh38
NC_000002.11:g.241808523G>A , CM000664.1:g.241808523G>A GRCh37
NC_000002.10:g.241457196G>A NCBI36
NG_008005.1:g.5362G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-64G>A MANE Select ENSP00000302620.3:n.166-64G>A
ENST00000307503.3:c.166-64G>A ENSP00000302620.3:n.166-64G>A
ENST00000472436.1:n.186-64G>A
NM_000030.2:c.166-64G>A NP_000021.1:n.166-64G>A
XR_924060.1:n.405+1127C>T
NM_000030.3:c.166-64G>A MANE Select NP_000021.1:n.166-64G>A