Canonical Allele Identifier: CA2664009473
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240875902-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875902T>A , CM000664.2:g.240875902T>A GRCh38
NC_000002.11:g.241815319T>A , CM000664.1:g.241815319T>A GRCh37
NC_000002.10:g.241463992T>A NCBI36
NG_008005.1:g.12158T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.777-33T>A MANE Select ENSP00000302620.3:n.777-33T>A
ENST00000307503.3:c.777-33T>A ENSP00000302620.3:n.777-33T>A
ENST00000476698.1:n.429-33T>A
NM_000030.2:c.777-33T>A NP_000021.1:n.777-33T>A
NM_000030.3:c.777-33T>A MANE Select NP_000021.1:n.777-33T>A
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