Canonical Allele Identifier: CA766960561
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1205821422

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869112G>C , CM000664.2:g.240869112G>C GRCh38
NC_000002.11:g.241808529G>C , CM000664.1:g.241808529G>C GRCh37
NC_000002.10:g.241457202G>C NCBI36
NG_008005.1:g.5368G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-58G>C MANE Select ENSP00000302620.3:n.166-58G>C
ENST00000307503.3:c.166-58G>C ENSP00000302620.3:n.166-58G>C
ENST00000472436.1:n.186-58G>C
NM_000030.2:c.166-58G>C NP_000021.1:n.166-58G>C
XR_924060.1:n.405+1121C>G
NM_000030.3:c.166-58G>C MANE Select NP_000021.1:n.166-58G>C