Canonical Allele Identifier: CA766957807
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1283863492
MyVariant Identifiers: chr2:g.241816670G>A (hg19) chr2:g.240877253G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877253G>A , CM000664.2:g.240877253G>A GRCh38
NC_000002.11:g.241816670G>A , CM000664.1:g.241816670G>A GRCh37
NC_000002.10:g.241465343G>A NCBI36
NG_008005.1:g.13509G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-284G>A MANE Select ENSP00000302620.3:n.847-284G>A
ENST00000307503.3:c.847-284G>A ENSP00000302620.3:n.847-284G>A
ENST00000470255.1:n.341G>A
NM_000030.2:c.847-284G>A NP_000021.1:n.847-284G>A
NM_000030.3:c.847-284G>A MANE Select NP_000021.1:n.847-284G>A
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