Canonical Allele Identifier: CA351312902
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868927C>A , CM000664.2:g.240868927C>A GRCh38
NC_000002.11:g.241808344C>A , CM000664.1:g.241808344C>A GRCh37
NC_000002.10:g.241457017C>A NCBI36
NG_008005.1:g.5183C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.62C>A MANE Select ENSP00000302620.3:p.Pro21His
ENST00000307503.3:c.62C>A ENSP00000302620.3:p.Pro21His
ENST00000472436.1:n.82C>A
NM_000030.2:c.62C>A NP_000021.1:p.Pro21His
XR_924060.1:n.405+1306G>T
NM_000030.3:c.62C>A MANE Select NP_000021.1:p.Pro21His