Canonical Allele Identifier: CA2664003859
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868728A>C , CM000664.2:g.240868728A>C GRCh38
NC_000002.11:g.241808145A>C , CM000664.1:g.241808145A>C GRCh37
NC_000002.10:g.241456818A>C NCBI36
NG_008005.1:g.4984A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-138A>C ENSP00000302620.3:n.-138A>C
XR_924060.1:n.405+1505T>G