Canonical Allele Identifier: CA1339335402
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059030960

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877364T>C , CM000664.2:g.240877364T>C GRCh38
NC_000002.11:g.241816781T>C , CM000664.1:g.241816781T>C GRCh37
NC_000002.10:g.241465454T>C NCBI36
NG_008005.1:g.13620T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-173T>C MANE Select ENSP00000302620.3:n.847-173T>C
ENST00000307503.3:c.847-173T>C ENSP00000302620.3:n.847-173T>C
ENST00000470255.1:n.452T>C
NM_000030.2:c.847-173T>C NP_000021.1:n.847-173T>C
NM_000030.3:c.847-173T>C MANE Select NP_000021.1:n.847-173T>C