Canonical Allele Identifier: CA2209022
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs778459277

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869137G>T , CM000664.2:g.240869137G>T GRCh38
NC_000002.11:g.241808554G>T , CM000664.1:g.241808554G>T GRCh37
NC_000002.10:g.241457227G>T NCBI36
NG_008005.1:g.5393G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-33G>T MANE Select ENSP00000302620.3:n.166-33G>T
ENST00000307503.3:c.166-33G>T ENSP00000302620.3:n.166-33G>T
ENST00000472436.1:n.186-33G>T
NM_000030.2:c.166-33G>T NP_000021.1:n.166-33G>T
XR_924060.1:n.405+1096C>A
NM_000030.3:c.166-33G>T MANE Select NP_000021.1:n.166-33G>T