Canonical Allele Identifier: CA1339335400
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877357T= , CM000664.2:g.240877357T= GRCh38
NC_000002.11:g.241816774T= , CM000664.1:g.241816774T= GRCh37
NC_000002.10:g.241465447T= NCBI36
NG_008005.1:g.13613T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-180T= MANE Select ENSP00000302620.3:n.847-180T=
ENST00000307503.3:c.847-180T= ENSP00000302620.3:n.847-180T=
ENST00000470255.1:n.445T=
NM_000030.2:c.847-180T= NP_000021.1:n.847-180T=
NM_000030.3:c.847-180T= MANE Select NP_000021.1:n.847-180T=