Canonical Allele Identifier: CA1339331029
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058979240

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869368G>A , CM000664.2:g.240869368G>A GRCh38
NC_000002.11:g.241808785G>A , CM000664.1:g.241808785G>A GRCh37
NC_000002.10:g.241457458G>A NCBI36
NG_008005.1:g.5624G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.358+6G>A MANE Select ENSP00000302620.3:n.358+6G>A
ENST00000307503.3:c.358+6G>A ENSP00000302620.3:n.358+6G>A
ENST00000472436.1:n.378+6G>A
NM_000030.2:c.358+6G>A NP_000021.1:n.358+6G>A
XR_924060.1:n.405+865C>T
NM_000030.3:c.358+6G>A MANE Select NP_000021.1:n.358+6G>A