Canonical Allele Identifier: CA1339330655
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058974069
gnomAD v4: 2-240868727-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868727C>A , CM000664.2:g.240868727C>A GRCh38
NC_000002.11:g.241808144C>A , CM000664.1:g.241808144C>A GRCh37
NC_000002.10:g.241456817C>A NCBI36
NG_008005.1:g.4983C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-139C>A ENSP00000302620.3:n.-139C>A
XR_924060.1:n.405+1506G>T
Search 100 bp 5'
Search 100 bp 3'