Canonical Allele Identifier: CA1339330683
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1575707034

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868775A>C , CM000664.2:g.240868775A>C GRCh38
NC_000002.11:g.241808192A>C , CM000664.1:g.241808192A>C GRCh37
NC_000002.10:g.241456865A>C NCBI36
NG_008005.1:g.5031A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-91A>C ENSP00000302620.3:n.-91A>C
NM_000030.2:c.-91A>C NP_000021.1:n.-91A>C
XR_924060.1:n.405+1458T>G