Canonical Allele Identifier: CA1339330679
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1575707032

Genomic Alleles

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

Transcript Alleles

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