Canonical Allele Identifier: CA1339334505
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1442572525

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875733C>G , CM000664.2:g.240875733C>G GRCh38
NC_000002.11:g.241815150C>G , CM000664.1:g.241815150C>G GRCh37
NC_000002.10:g.241463823C>G NCBI36
NG_008005.1:g.11989C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.777-202C>G MANE Select ENSP00000302620.3:n.777-202C>G
ENST00000307503.3:c.777-202C>G ENSP00000302620.3:n.777-202C>G
ENST00000476698.1:n.429-202C>G
NM_000030.2:c.777-202C>G NP_000021.1:n.777-202C>G
NM_000030.3:c.777-202C>G MANE Select NP_000021.1:n.777-202C>G