Canonical Allele Identifier: CA1339330563
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058973158

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868534C>G , CM000664.2:g.240868534C>G GRCh38
NC_000002.11:g.241807951C>G , CM000664.1:g.241807951C>G GRCh37
NC_000002.10:g.241456624C>G NCBI36
NG_008005.1:g.4790C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-332C>G ENSP00000302620.3:n.-332C>G
XR_924060.1:n.405+1699G>C