Canonical Allele Identifier: CA766957934
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1310383471

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877524A>T , CM000664.2:g.240877524A>T GRCh38
NC_000002.11:g.241816941A>T , CM000664.1:g.241816941A>T GRCh37
NC_000002.10:g.241465614A>T NCBI36
NG_008005.1:g.13780A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-13A>T MANE Select ENSP00000302620.3:n.847-13A>T
ENST00000307503.3:c.847-13A>T ENSP00000302620.3:n.847-13A>T
ENST00000470255.1:n.612A>T
NM_000030.2:c.847-13A>T NP_000021.1:n.847-13A>T
NM_000030.3:c.847-13A>T MANE Select NP_000021.1:n.847-13A>T