Canonical Allele Identifier: CA1339335659
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877858C= , CM000664.2:g.240877858C= GRCh38
NC_000002.11:g.241817275C= , CM000664.1:g.241817275C= GRCh37
NC_000002.10:g.241465948C= NCBI36
NG_008005.1:g.14114C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-164C= MANE Select ENSP00000302620.3:n.943-164C=
ENST00000307503.3:c.943-164C= ENSP00000302620.3:n.943-164C=
ENST00000470255.1:n.721-164C=
NM_000030.2:c.943-164C= NP_000021.1:n.943-164C=
NM_000030.3:c.943-164C= MANE Select NP_000021.1:n.943-164C=
Search 100 bp 5'
Search 100 bp 3'