Canonical Allele Identifier: CA2209008
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs770314210

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869075C>T , CM000664.2:g.240869075C>T GRCh38
NC_000002.11:g.241808492C>T , CM000664.1:g.241808492C>T GRCh37
NC_000002.10:g.241457165C>T NCBI36
NG_008005.1:g.5331C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+45C>T MANE Select ENSP00000302620.3:n.165+45C>T
ENST00000307503.3:c.165+45C>T ENSP00000302620.3:n.165+45C>T
ENST00000472436.1:n.185+45C>T
NM_000030.2:c.165+45C>T NP_000021.1:n.165+45C>T
XR_924060.1:n.405+1158G>A
NM_000030.3:c.165+45C>T MANE Select NP_000021.1:n.165+45C>T