Canonical Allele Identifier: CA1339336347
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059044605
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879206C>T , CM000664.2:g.240879206C>T GRCh38
NC_000002.11:g.241818623C>T , CM000664.1:g.241818623C>T GRCh37
NC_000002.10:g.241467296C>T NCBI36
NG_008005.1:g.15462C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*385C>T MANE Select ENSP00000302620.3:n.*385C>T
ENST00000470255.1:n.1342C>T
NM_000030.3:c.*385C>T MANE Select NP_000021.1:n.*385C>T
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