Canonical Allele Identifier: CA1515648947
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs776742063

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442198C>G , CM000666.2:g.177442198C>G GRCh38
NC_000004.11:g.178363352C>G , CM000666.1:g.178363352C>G GRCh37
NC_000004.10:g.178600346C>G NCBI36
NG_011845.2:g.5306G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.127+51G>C MANE Select ENSP00000264595.2:n.127+51G>C
ENST00000264595.6:c.127+51G>C ENSP00000264595.2:n.127+51G>C
ENST00000506853.5:n.161+51G>C
ENST00000510955.5:n.161+51G>C
ENST00000511231.1:n.161+51G>C
NM_000027.3:c.127+51G>C NP_000018.2:n.127+51G>C
NM_001171988.1:c.127+51G>C NP_001165459.1:n.127+51G>C
NR_033655.1:n.255+51G>C
XM_006714123.2:c.127+51G>C XP_006714186.1:n.127+51G>C
XR_001741155.2:n.221+51G>C
NM_000027.4:c.127+51G>C MANE Select NP_000018.2:n.127+51G>C
NM_001171988.2:c.127+51G>C NP_001165459.1:n.127+51G>C
NR_033655.2:n.189+51G>C