Canonical Allele Identifier: CA351313765
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1255185630

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869304C>A , CM000664.2:g.240869304C>A GRCh38
NC_000002.11:g.241808721C>A , CM000664.1:g.241808721C>A GRCh37
NC_000002.10:g.241457394C>A NCBI36
NG_008005.1:g.5560C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.300C>A MANE Select ENSP00000302620.3:p.Phe100Leu
ENST00000307503.3:c.300C>A ENSP00000302620.3:p.Phe100Leu
ENST00000472436.1:n.320C>A
NM_000030.2:c.300C>A NP_000021.1:p.Phe100Leu
XR_924060.1:n.405+929G>T
NM_000030.3:c.300C>A MANE Select NP_000021.1:p.Phe100Leu