Canonical Allele Identifier: CA1515648931
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1737049932

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442194T>G , CM000666.2:g.177442194T>G GRCh38
NC_000004.11:g.178363348T>G , CM000666.1:g.178363348T>G GRCh37
NC_000004.10:g.178600342T>G NCBI36
NG_011845.2:g.5310A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.127+55A>C MANE Select ENSP00000264595.2:n.127+55A>C
ENST00000264595.6:c.127+55A>C ENSP00000264595.2:n.127+55A>C
ENST00000506853.5:n.161+55A>C
ENST00000510955.5:n.161+55A>C
ENST00000511231.1:n.161+55A>C
NM_000027.3:c.127+55A>C NP_000018.2:n.127+55A>C
NM_001171988.1:c.127+55A>C NP_001165459.1:n.127+55A>C
NR_033655.1:n.255+55A>C
XM_006714123.2:c.127+55A>C XP_006714186.1:n.127+55A>C
XR_001741155.2:n.221+55A>C
NM_000027.4:c.127+55A>C MANE Select NP_000018.2:n.127+55A>C
NM_001171988.2:c.127+55A>C NP_001165459.1:n.127+55A>C
NR_033655.2:n.189+55A>C