Canonical Allele Identifier: CA2664003898
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240868744-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868744A>C , CM000664.2:g.240868744A>C GRCh38
NC_000002.11:g.241808161A>C , CM000664.1:g.241808161A>C GRCh37
NC_000002.10:g.241456834A>C NCBI36
NG_008005.1:g.5000A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-122A>C ENSP00000302620.3:n.-122A>C
XR_924060.1:n.405+1489T>G
Search 100 bp 5'
Search 100 bp 3'