Canonical Allele Identifier: CA1339336057
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059040639
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878558C>A , CM000664.2:g.240878558C>A GRCh38
NC_000002.11:g.241817975C>A , CM000664.1:g.241817975C>A GRCh37
NC_000002.10:g.241466648C>A NCBI36
NG_008005.1:g.14814C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-156C>A MANE Select ENSP00000302620.3:n.1072-156C>A
ENST00000307503.3:c.1072-156C>A ENSP00000302620.3:n.1072-156C>A
ENST00000470255.1:n.850-156C>A
NM_000030.2:c.1072-156C>A NP_000021.1:n.1072-156C>A
NM_000030.3:c.1072-156C>A MANE Select NP_000021.1:n.1072-156C>A
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