Canonical Allele Identifier: CA2664004176
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240868829-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868829A>T , CM000664.2:g.240868829A>T GRCh38
NC_000002.11:g.241808246A>T , CM000664.1:g.241808246A>T GRCh37
NC_000002.10:g.241456919A>T NCBI36
NG_008005.1:g.5085A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-37A>T MANE Select ENSP00000302620.3:n.-37A>T
ENST00000307503.3:c.-37A>T ENSP00000302620.3:n.-37A>T
NM_000030.2:c.-37A>T NP_000021.1:n.-37A>T
XR_924060.1:n.405+1404T>A
NM_000030.3:c.-37A>T MANE Select NP_000021.1:n.-37A>T
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