Canonical Allele Identifier: CA2672748416
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440528G>A , CM000666.2:g.177440528G>A GRCh38
NC_000004.11:g.178361682G>A , CM000666.1:g.178361682G>A GRCh37
NC_000004.10:g.178598676G>A NCBI36
NG_011845.2:g.6976C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.128-102C>T MANE Select ENSP00000264595.2:n.128-102C>T
ENST00000264595.6:c.128-102C>T ENSP00000264595.2:n.128-102C>T
ENST00000506853.5:n.162-102C>T
ENST00000510955.5:n.162-102C>T
ENST00000511231.1:n.162-102C>T
NM_000027.3:c.128-102C>T NP_000018.2:n.128-102C>T
NM_001171988.1:c.128-102C>T NP_001165459.1:n.128-102C>T
NR_033655.1:n.256-102C>T
XM_006714123.2:c.128-102C>T XP_006714186.1:n.128-102C>T
XR_001741155.2:n.222-102C>T
NM_000027.4:c.128-102C>T MANE Select NP_000018.2:n.128-102C>T
NM_001171988.2:c.128-102C>T NP_001165459.1:n.128-102C>T
NR_033655.2:n.190-102C>T