Canonical Allele Identifier: CA1339330652
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058974053

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868721A>G , CM000664.2:g.240868721A>G GRCh38
NC_000002.11:g.241808138A>G , CM000664.1:g.241808138A>G GRCh37
NC_000002.10:g.241456811A>G NCBI36
NG_008005.1:g.4977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-145A>G ENSP00000302620.3:n.-145A>G
XR_924060.1:n.405+1512T>C