Canonical Allele Identifier: CA1339330708
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868832C= , CM000664.2:g.240868832C= GRCh38
NC_000002.11:g.241808249C= , CM000664.1:g.241808249C= GRCh37
NC_000002.10:g.241456922C= NCBI36
NG_008005.1:g.5088C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-34C= MANE Select ENSP00000302620.3:n.-34C=
ENST00000307503.3:c.-34C= ENSP00000302620.3:n.-34C=
NM_000030.2:c.-34C= NP_000021.1:n.-34C=
XR_924060.1:n.405+1401G=
NM_000030.3:c.-34C= MANE Select NP_000021.1:n.-34C=