Canonical Allele Identifier: CA351319292
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241817021T>A (hg19) chr2:g.240877604T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877604T>A , CM000664.2:g.240877604T>A GRCh38
NC_000002.11:g.241817021T>A , CM000664.1:g.241817021T>A GRCh37
NC_000002.10:g.241465694T>A NCBI36
NG_008005.1:g.13860T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.914T>A MANE Select ENSP00000302620.3:p.Leu305Gln
ENST00000307503.3:c.914T>A ENSP00000302620.3:p.Leu305Gln
ENST00000470255.1:n.692T>A
NM_000030.2:c.914T>A NP_000021.1:p.Leu305Gln
NM_000030.3:c.914T>A MANE Select NP_000021.1:p.Leu305Gln
Search 100 bp 5'
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