Canonical Allele Identifier: CA1071331020
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1736967715

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440604T>C , CM000666.2:g.177440604T>C GRCh38
NC_000004.11:g.178361758T>C , CM000666.1:g.178361758T>C GRCh37
NC_000004.10:g.178598752T>C NCBI36
NG_011845.2:g.6900A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.128-178A>G MANE Select ENSP00000264595.2:n.128-178A>G
ENST00000264595.6:c.128-178A>G ENSP00000264595.2:n.128-178A>G
ENST00000506853.5:n.162-178A>G
ENST00000510955.5:n.162-178A>G
ENST00000511231.1:n.162-178A>G
NM_000027.3:c.128-178A>G NP_000018.2:n.128-178A>G
NM_001171988.1:c.128-178A>G NP_001165459.1:n.128-178A>G
NR_033655.1:n.256-178A>G
XM_006714123.2:c.128-178A>G XP_006714186.1:n.128-178A>G
XR_001741155.2:n.222-178A>G
NM_000027.4:c.128-178A>G MANE Select NP_000018.2:n.128-178A>G
NM_001171988.2:c.128-178A>G NP_001165459.1:n.128-178A>G
NR_033655.2:n.190-178A>G