Canonical Allele Identifier: CA2664003895
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868743C>T , CM000664.2:g.240868743C>T GRCh38
NC_000002.11:g.241808160C>T , CM000664.1:g.241808160C>T GRCh37
NC_000002.10:g.241456833C>T NCBI36
NG_008005.1:g.4999C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-123C>T ENSP00000302620.3:n.-123C>T
XR_924060.1:n.405+1490G>A