Canonical Allele Identifier: CA351319472
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878031C>T , CM000664.2:g.240878031C>T GRCh38
NC_000002.11:g.241817448C>T , CM000664.1:g.241817448C>T GRCh37
NC_000002.10:g.241466121C>T NCBI36
NG_008005.1:g.14287C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.952C>T MANE Select ENSP00000302620.3:p.Leu318Phe
ENST00000307503.3:c.952C>T ENSP00000302620.3:p.Leu318Phe
ENST00000470255.1:n.730C>T
NM_000030.2:c.952C>T NP_000021.1:p.Leu318Phe
NM_000030.3:c.952C>T MANE Select NP_000021.1:p.Leu318Phe