Canonical Allele Identifier: CA2672748400
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440495C>A , CM000666.2:g.177440495C>A GRCh38
NC_000004.11:g.178361649C>A , CM000666.1:g.178361649C>A GRCh37
NC_000004.10:g.178598643C>A NCBI36
NG_011845.2:g.7009G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.128-69G>T MANE Select ENSP00000264595.2:n.128-69G>T
ENST00000264595.6:c.128-69G>T ENSP00000264595.2:n.128-69G>T
ENST00000506853.5:n.162-69G>T
ENST00000510955.5:n.162-69G>T
ENST00000511231.1:n.162-69G>T
NM_000027.3:c.128-69G>T NP_000018.2:n.128-69G>T
NM_001171988.1:c.128-69G>T NP_001165459.1:n.128-69G>T
NR_033655.1:n.256-69G>T
XM_006714123.2:c.128-69G>T XP_006714186.1:n.128-69G>T
XR_001741155.2:n.222-69G>T
NM_000027.4:c.128-69G>T MANE Select NP_000018.2:n.128-69G>T
NM_001171988.2:c.128-69G>T NP_001165459.1:n.128-69G>T
NR_033655.2:n.190-69G>T