Canonical Allele Identifier: CA1339330665
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868745C= , CM000664.2:g.240868745C= GRCh38
NC_000002.11:g.241808162C= , CM000664.1:g.241808162C= GRCh37
NC_000002.10:g.241456835C= NCBI36
NG_008005.1:g.5001C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-121C= ENSP00000302620.3:n.-121C=
NM_000030.2:c.-121C= NP_000021.1:n.-121C=
XR_924060.1:n.405+1488G=