Canonical Allele Identifier: CA1339335405
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877372T= , CM000664.2:g.240877372T= GRCh38
NC_000002.11:g.241816789T= , CM000664.1:g.241816789T= GRCh37
NC_000002.10:g.241465462T= NCBI36
NG_008005.1:g.13628T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-165T= MANE Select ENSP00000302620.3:n.847-165T=
ENST00000307503.3:c.847-165T= ENSP00000302620.3:n.847-165T=
ENST00000470255.1:n.460T=
NM_000030.2:c.847-165T= NP_000021.1:n.847-165T=
NM_000030.3:c.847-165T= MANE Select NP_000021.1:n.847-165T=