Canonical Allele Identifier: CA358783467
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438841T>A , CM000666.2:g.177438841T>A GRCh38
NC_000004.11:g.178359995T>A , CM000666.1:g.178359995T>A GRCh37
NC_000004.10:g.178596989T>A NCBI36
NG_011845.2:g.8663A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.411A>T MANE Select ENSP00000264595.2:p.Gln137His
ENST00000264595.6:c.411A>T ENSP00000264595.2:p.Gln137His
ENST00000502310.5:c.66A>T ENSP00000423798.1:p.Gln22His
ENST00000506853.5:n.445A>T
ENST00000510635.1:c.107A>T
ENST00000510955.5:n.332A>T
NM_000027.3:c.411A>T NP_000018.2:p.Gln137His
NM_001171988.1:c.411A>T NP_001165459.1:p.Gln137His
NR_033655.1:n.539A>T
XM_006714123.2:c.411A>T XP_006714186.1:p.Gln137His
XR_001741155.2:n.505A>T
NM_000027.4:c.411A>T MANE Select NP_000018.2:p.Gln137His
NM_001171988.2:c.411A>T NP_001165459.1:p.Gln137His
NR_033655.2:n.473A>T