Canonical Allele Identifier: CA1339335491
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877525T= , CM000664.2:g.240877525T= GRCh38
NC_000002.11:g.241816942T= , CM000664.1:g.241816942T= GRCh37
NC_000002.10:g.241465615T= NCBI36
NG_008005.1:g.13781T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-12T= MANE Select ENSP00000302620.3:n.847-12T=
ENST00000307503.3:c.847-12T= ENSP00000302620.3:n.847-12T=
ENST00000470255.1:n.613T=
NM_000030.2:c.847-12T= NP_000021.1:n.847-12T=
NM_000030.3:c.847-12T= MANE Select NP_000021.1:n.847-12T=
Search 100 bp 5'
Search 100 bp 3'