Canonical Allele Identifier: CA351312534
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1559567678
gnomAD v4: 2-240868877-C-G
MyVariant Identifiers: chr2:g.241808294C>G (hg19) chr2:g.240868877C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868877C>G , CM000664.2:g.240868877C>G GRCh38
NC_000002.11:g.241808294C>G , CM000664.1:g.241808294C>G GRCh37
NC_000002.10:g.241456967C>G NCBI36
NG_008005.1:g.5133C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.12C>G MANE Select ENSP00000302620.3:p.His4Gln
ENST00000307503.3:c.12C>G ENSP00000302620.3:p.His4Gln
ENST00000472436.1:n.32C>G
NM_000030.2:c.12C>G NP_000021.1:p.His4Gln
XR_924060.1:n.405+1356G>C
NM_000030.3:c.12C>G MANE Select NP_000021.1:p.His4Gln
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