Canonical Allele Identifier: CA1339330668
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868750G= , CM000664.2:g.240868750G= GRCh38
NC_000002.11:g.241808167G= , CM000664.1:g.241808167G= GRCh37
NC_000002.10:g.241456840G= NCBI36
NG_008005.1:g.5006G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-116G= ENSP00000302620.3:n.-116G=
NM_000030.2:c.-116G= NP_000021.1:n.-116G=
XR_924060.1:n.405+1483C=