Canonical Allele Identifier: CA351313431
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869209C>A , CM000664.2:g.240869209C>A GRCh38
NC_000002.11:g.241808626C>A , CM000664.1:g.241808626C>A GRCh37
NC_000002.10:g.241457299C>A NCBI36
NG_008005.1:g.5465C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.205C>A MANE Select ENSP00000302620.3:p.Gln69Lys
ENST00000307503.3:c.205C>A ENSP00000302620.3:p.Gln69Lys
ENST00000472436.1:n.225C>A
NM_000030.2:c.205C>A NP_000021.1:p.Gln69Lys
XR_924060.1:n.405+1024G>T
NM_000030.3:c.205C>A MANE Select NP_000021.1:p.Gln69Lys