Canonical Allele Identifier: CA1339330580
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868567T= , CM000664.2:g.240868567T= GRCh38
NC_000002.11:g.241807984T= , CM000664.1:g.241807984T= GRCh37
NC_000002.10:g.241456657T= NCBI36
NG_008005.1:g.4823T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-299T= ENSP00000302620.3:n.-299T=
XR_924060.1:n.405+1666A=