Canonical Allele Identifier: CA1339330675
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1559567602

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868768A>T , CM000664.2:g.240868768A>T GRCh38
NC_000002.11:g.241808185A>T , CM000664.1:g.241808185A>T GRCh37
NC_000002.10:g.241456858A>T NCBI36
NG_008005.1:g.5024A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-98A>T ENSP00000302620.3:n.-98A>T
NM_000030.2:c.-98A>T NP_000021.1:n.-98A>T
XR_924060.1:n.405+1465T>A