Canonical Allele Identifier: CA68173641
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs139677440

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869095G>A , CM000664.2:g.240869095G>A GRCh38
NC_000002.11:g.241808512G>A , CM000664.1:g.241808512G>A GRCh37
NC_000002.10:g.241457185G>A NCBI36
NG_008005.1:g.5351G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+65G>A MANE Select ENSP00000302620.3:n.165+65G>A
ENST00000307503.3:c.165+65G>A ENSP00000302620.3:n.165+65G>A
ENST00000472436.1:n.185+65G>A
NM_000030.2:c.165+65G>A NP_000021.1:n.165+65G>A
XR_924060.1:n.405+1138C>T
NM_000030.3:c.165+65G>A MANE Select NP_000021.1:n.165+65G>A