Canonical Allele Identifier: CA766964122
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1344681677
gnomAD v3: 2-240873928-C-T
gnomAD v4: 2-240873928-C-T
MyVariant Identifiers: chr2:g.241813345C>T (hg19) chr2:g.240873928C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873928C>T , CM000664.2:g.240873928C>T GRCh38
NC_000002.11:g.241813345C>T , CM000664.1:g.241813345C>T GRCh37
NC_000002.10:g.241462018C>T NCBI36
NG_008005.1:g.10184C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-50C>T MANE Select ENSP00000302620.3:n.596-50C>T
ENST00000307503.3:c.596-50C>T ENSP00000302620.3:n.596-50C>T
ENST00000476698.1:n.332+879C>T
NM_000030.2:c.596-50C>T NP_000021.1:n.596-50C>T
NM_000030.3:c.596-50C>T MANE Select NP_000021.1:n.596-50C>T
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