Canonical Allele Identifier: CA1339330702
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868822C= , CM000664.2:g.240868822C= GRCh38
NC_000002.11:g.241808239C= , CM000664.1:g.241808239C= GRCh37
NC_000002.10:g.241456912C= NCBI36
NG_008005.1:g.5078C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-44C= ENSP00000302620.3:n.-44C=
NM_000030.2:c.-44C= NP_000021.1:n.-44C=
XR_924060.1:n.405+1411G=