Canonical Allele Identifier: CA351319766
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241818158A>C (hg19) chr2:g.240878741A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878741A>C , CM000664.2:g.240878741A>C GRCh38
NC_000002.11:g.241818158A>C , CM000664.1:g.241818158A>C GRCh37
NC_000002.10:g.241466831A>C NCBI36
NG_008005.1:g.14997A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1099A>C MANE Select ENSP00000302620.3:p.Asn367His
ENST00000307503.3:c.1099A>C ENSP00000302620.3:p.Asn367His
ENST00000470255.1:n.877A>C
NM_000030.2:c.1099A>C NP_000021.1:p.Asn367His
NM_000030.3:c.1099A>C MANE Select NP_000021.1:p.Asn367His
Search 100 bp 5'
Search 100 bp 3'