Canonical Allele Identifier: CA2664004261
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240868847-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868847G>C , CM000664.2:g.240868847G>C GRCh38
NC_000002.11:g.241808264G>C , CM000664.1:g.241808264G>C GRCh37
NC_000002.10:g.241456937G>C NCBI36
NG_008005.1:g.5103G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-19G>C MANE Select ENSP00000302620.3:n.-19G>C
ENST00000307503.3:c.-19G>C ENSP00000302620.3:n.-19G>C
ENST00000472436.1:n.2G>C
NM_000030.2:c.-19G>C NP_000021.1:n.-19G>C
XR_924060.1:n.405+1386C>G
NM_000030.3:c.-19G>C MANE Select NP_000021.1:n.-19G>C
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