Canonical Allele Identifier: CA2664003994
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1575707032

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868769C>A , CM000664.2:g.240868769C>A GRCh38
NC_000002.11:g.241808186C>A , CM000664.1:g.241808186C>A GRCh37
NC_000002.10:g.241456859C>A NCBI36
NG_008005.1:g.5025C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-97C>A ENSP00000302620.3:n.-97C>A
NM_000030.2:c.-97C>A NP_000021.1:n.-97C>A
XR_924060.1:n.405+1464G>T