Canonical Allele Identifier: CA1339335219
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877033C= , CM000664.2:g.240877033C= GRCh38
NC_000002.11:g.241816450C= , CM000664.1:g.241816450C= GRCh37
NC_000002.10:g.241465123C= NCBI36
NG_008005.1:g.13289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-504C= MANE Select ENSP00000302620.3:n.847-504C=
ENST00000307503.3:c.847-504C= ENSP00000302620.3:n.847-504C=
ENST00000470255.1:n.121C=
NM_000030.2:c.847-504C= NP_000021.1:n.847-504C=
NM_000030.3:c.847-504C= MANE Select NP_000021.1:n.847-504C=