Canonical Allele Identifier: CA1339334140
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059015816

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875069A>T , CM000664.2:g.240875069A>T GRCh38
NC_000002.11:g.241814486A>T , CM000664.1:g.241814486A>T GRCh37
NC_000002.10:g.241463159A>T NCBI36
NG_008005.1:g.11325A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-40A>T MANE Select ENSP00000302620.3:n.681-40A>T
ENST00000307503.3:c.681-40A>T ENSP00000302620.3:n.681-40A>T
ENST00000476698.1:n.333-40A>T
NM_000030.2:c.681-40A>T NP_000021.1:n.681-40A>T
NM_000030.3:c.681-40A>T MANE Select NP_000021.1:n.681-40A>T