Canonical Allele Identifier: CA2672747488
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438742T>C , CM000666.2:g.177438742T>C GRCh38
NC_000004.11:g.178359896T>C , CM000666.1:g.178359896T>C GRCh37
NC_000004.10:g.178596890T>C NCBI36
NG_011845.2:g.8762A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.507+3A>G MANE Select ENSP00000264595.2:n.507+3A>G
ENST00000264595.6:c.507+3A>G ENSP00000264595.2:n.507+3A>G
ENST00000502310.5:c.162+3A>G ENSP00000423798.1:n.162+3A>G
ENST00000506853.5:n.541+3A>G
ENST00000510635.1:c.203+3A>G
ENST00000510955.5:n.428+3A>G
NM_000027.3:c.507+3A>G NP_000018.2:n.507+3A>G
NM_001171988.1:c.507+3A>G NP_001165459.1:n.507+3A>G
NR_033655.1:n.635+3A>G
XM_006714123.2:c.507+3A>G XP_006714186.1:n.507+3A>G
XR_001741155.2:n.601+3A>G
NM_000027.4:c.507+3A>G MANE Select NP_000018.2:n.507+3A>G
NM_001171988.2:c.507+3A>G NP_001165459.1:n.507+3A>G
NR_033655.2:n.569+3A>G