Canonical Allele Identifier: CA540538864
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1482105511

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878709C>G , CM000664.2:g.240878709C>G GRCh38
NC_000002.11:g.241818126C>G , CM000664.1:g.241818126C>G GRCh37
NC_000002.10:g.241466799C>G NCBI36
NG_008005.1:g.14965C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-5C>G MANE Select ENSP00000302620.3:n.1072-5C>G
ENST00000307503.3:c.1072-5C>G ENSP00000302620.3:n.1072-5C>G
ENST00000470255.1:n.850-5C>G
NM_000030.2:c.1072-5C>G NP_000021.1:n.1072-5C>G
NM_000030.3:c.1072-5C>G MANE Select NP_000021.1:n.1072-5C>G