Canonical Allele Identifier: CA2664012217
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106432325
gnomAD v4: 2-240878607-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878607G>A , CM000664.2:g.240878607G>A GRCh38
NC_000002.11:g.241818024G>A , CM000664.1:g.241818024G>A GRCh37
NC_000002.10:g.241466697G>A NCBI36
NG_008005.1:g.14863G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-107G>A MANE Select ENSP00000302620.3:n.1072-107G>A
ENST00000307503.3:c.1072-107G>A ENSP00000302620.3:n.1072-107G>A
ENST00000470255.1:n.850-107G>A
NM_000030.2:c.1072-107G>A NP_000021.1:n.1072-107G>A
NM_000030.3:c.1072-107G>A MANE Select NP_000021.1:n.1072-107G>A
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