Canonical Allele Identifier: CA2577302581
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240872924T>C , CM000664.2:g.240872924T>C GRCh38
NC_000002.11:g.241812341T>C , CM000664.1:g.241812341T>C GRCh37
NC_000002.10:g.241461014T>C NCBI36
NG_008005.1:g.9180T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.525-55T>C MANE Select ENSP00000302620.3:n.525-55T>C
ENST00000307503.3:c.525-55T>C ENSP00000302620.3:n.525-55T>C
ENST00000472436.1:n.545-55T>C
ENST00000476698.1:n.262-55T>C
NM_000030.2:c.525-55T>C NP_000021.1:n.525-55T>C
NM_000030.3:c.525-55T>C MANE Select NP_000021.1:n.525-55T>C