Canonical Allele Identifier: CA1339330568
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs960376038

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868538G>C , CM000664.2:g.240868538G>C GRCh38
NC_000002.11:g.241807955G>C , CM000664.1:g.241807955G>C GRCh37
NC_000002.10:g.241456628G>C NCBI36
NG_008005.1:g.4794G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-328G>C ENSP00000302620.3:n.-328G>C
XR_924060.1:n.405+1695C>G