Canonical Allele Identifier: CA2664003961
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240868763-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868763T>A , CM000664.2:g.240868763T>A GRCh38
NC_000002.11:g.241808180T>A , CM000664.1:g.241808180T>A GRCh37
NC_000002.10:g.241456853T>A NCBI36
NG_008005.1:g.5019T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-103T>A ENSP00000302620.3:n.-103T>A
NM_000030.2:c.-103T>A NP_000021.1:n.-103T>A
XR_924060.1:n.405+1470A>T
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