Canonical Allele Identifier: CA432024002
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1237384369
MyVariant Identifiers: chr2:g.241812447C>G (hg19) chr2:g.240873030C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873030C>G , CM000664.2:g.240873030C>G GRCh38
NC_000002.11:g.241812447C>G , CM000664.1:g.241812447C>G GRCh37
NC_000002.10:g.241461120C>G NCBI36
NG_008005.1:g.9286C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.576C>G MANE Select ENSP00000302620.3:p.Pro192=
ENST00000307503.3:c.576C>G ENSP00000302620.3:p.Pro192=
ENST00000472436.1:n.596C>G
ENST00000476698.1:n.313C>G
NM_000030.2:c.576C>G NP_000021.1:p.Pro192=
NM_000030.3:c.576C>G MANE Select NP_000021.1:p.Pro192=
Search 100 bp 5'
Search 100 bp 3'