Canonical Allele Identifier: CA358783720
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439642T>G , CM000666.2:g.177439642T>G GRCh38
NC_000004.11:g.178360796T>G , CM000666.1:g.178360796T>G GRCh37
NC_000004.10:g.178597790T>G NCBI36
NG_011845.2:g.7862A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.328A>C MANE Select ENSP00000264595.2:p.Asn110His
ENST00000264595.6:c.328A>C ENSP00000264595.2:p.Asn110His
ENST00000506853.5:n.362A>C
ENST00000510635.1:c.24A>C
ENST00000510955.5:n.315+631A>C
NM_000027.3:c.328A>C NP_000018.2:p.Asn110His
NM_001171988.1:c.328A>C NP_001165459.1:p.Asn110His
NR_033655.1:n.456A>C
XM_006714123.2:c.328A>C XP_006714186.1:p.Asn110His
XR_001741155.2:n.422A>C
NM_000027.4:c.328A>C MANE Select NP_000018.2:p.Asn110His
NM_001171988.2:c.328A>C NP_001165459.1:p.Asn110His
NR_033655.2:n.390A>C