Canonical Allele Identifier: CA68179682
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs376938355

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875091C>G , CM000664.2:g.240875091C>G GRCh38
NC_000002.11:g.241814508C>G , CM000664.1:g.241814508C>G GRCh37
NC_000002.10:g.241463181C>G NCBI36
NG_008005.1:g.11347C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-18C>G MANE Select ENSP00000302620.3:n.681-18C>G
ENST00000307503.3:c.681-18C>G ENSP00000302620.3:n.681-18C>G
ENST00000476698.1:n.333-18C>G
NM_000030.2:c.681-18C>G NP_000021.1:n.681-18C>G
NM_000030.3:c.681-18C>G MANE Select NP_000021.1:n.681-18C>G