Canonical Allele Identifier: CA351313855
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs796052060

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869328G>C , CM000664.2:g.240869328G>C GRCh38
NC_000002.11:g.241808745G>C , CM000664.1:g.241808745G>C GRCh37
NC_000002.10:g.241457418G>C NCBI36
NG_008005.1:g.5584G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.324G>C MANE Select ENSP00000302620.3:p.Trp108Cys
ENST00000307503.3:c.324G>C ENSP00000302620.3:p.Trp108Cys
ENST00000472436.1:n.344G>C
NM_000030.2:c.324G>C NP_000021.1:p.Trp108Cys
XR_924060.1:n.405+905C>G
NM_000030.3:c.324G>C MANE Select NP_000021.1:p.Trp108Cys