Canonical Allele Identifier: CA1339330564
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868536C= , CM000664.2:g.240868536C= GRCh38
NC_000002.11:g.241807953C= , CM000664.1:g.241807953C= GRCh37
NC_000002.10:g.241456626C= NCBI36
NG_008005.1:g.4792C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-330C= ENSP00000302620.3:n.-330C=
XR_924060.1:n.405+1697G=