Canonical Allele Identifier: CA2701683038
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058974134
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868741G>A , CM000664.2:g.240868741G>A GRCh38
NC_000002.11:g.241808158G>A , CM000664.1:g.241808158G>A GRCh37
NC_000002.10:g.241456831G>A NCBI36
NG_008005.1:g.4997G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-125G>A ENSP00000302620.3:n.-125G>A
XR_924060.1:n.405+1492C>T
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