Canonical Allele Identifier: CA432023982
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873024-G-C
MyVariant Identifiers: chr2:g.241812441G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873024G>C , CM000664.2:g.240873024G>C GRCh38
NC_000002.11:g.241812441G>C , CM000664.1:g.241812441G>C GRCh37
NC_000002.10:g.241461114G>C NCBI36
NG_008005.1:g.9280G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.570G>C MANE Select ENSP00000302620.3:p.Gly190=
ENST00000307503.3:c.570G>C ENSP00000302620.3:p.Gly190=
ENST00000472436.1:n.590G>C
ENST00000476698.1:n.307G>C
NM_000030.2:c.570G>C NP_000021.1:p.Gly190=
NM_000030.3:c.570G>C MANE Select NP_000021.1:p.Gly190=
Search 100 bp 5'
Search 100 bp 3'