Canonical Allele Identifier: CA351313942
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808763C>G (hg19) chr2:g.240869346C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869346C>G , CM000664.2:g.240869346C>G GRCh38
NC_000002.11:g.241808763C>G , CM000664.1:g.241808763C>G GRCh37
NC_000002.10:g.241457436C>G NCBI36
NG_008005.1:g.5602C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.342C>G MANE Select ENSP00000302620.3:p.Asp114Glu
ENST00000307503.3:c.342C>G ENSP00000302620.3:p.Asp114Glu
ENST00000472436.1:n.362C>G
NM_000030.2:c.342C>G NP_000021.1:p.Asp114Glu
XR_924060.1:n.405+887G>C
NM_000030.3:c.342C>G MANE Select NP_000021.1:p.Asp114Glu
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