Canonical Allele Identifier: CA2209106
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs180177232

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871444C>G , CM000664.2:g.240871444C>G GRCh38
NC_000002.11:g.241810861C>G , CM000664.1:g.241810861C>G GRCh37
NC_000002.10:g.241459534C>G NCBI36
NG_008005.1:g.7700C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.519C>G MANE Select ENSP00000302620.3:p.Cys173Trp
ENST00000307503.3:c.519C>G ENSP00000302620.3:p.Cys173Trp
ENST00000472436.1:n.539C>G
ENST00000476698.1:n.256C>G
NM_000030.2:c.519C>G NP_000021.1:p.Cys173Trp
NM_000030.3:c.519C>G MANE Select NP_000021.1:p.Cys173Trp