Canonical Allele Identifier: CA1339333451
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1575709720

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873796T>G , CM000664.2:g.240873796T>G GRCh38
NC_000002.11:g.241813213T>G , CM000664.1:g.241813213T>G GRCh37
NC_000002.10:g.241461886T>G NCBI36
NG_008005.1:g.10052T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-182T>G MANE Select ENSP00000302620.3:n.596-182T>G
ENST00000307503.3:c.596-182T>G ENSP00000302620.3:n.596-182T>G
ENST00000476698.1:n.332+747T>G
NM_000030.2:c.596-182T>G NP_000021.1:n.596-182T>G
NM_000030.3:c.596-182T>G MANE Select NP_000021.1:n.596-182T>G