Canonical Allele Identifier: CA791504077
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs746130532

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442411C>T , CM000666.2:g.177442411C>T GRCh38
NC_000004.11:g.178363565C>T , CM000666.1:g.178363565C>T GRCh37
NC_000004.10:g.178600559C>T NCBI36
NG_011845.2:g.5093G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-36G>A MANE Select ENSP00000264595.2:n.-36G>A
ENST00000264595.6:c.-36G>A ENSP00000264595.2:n.-36G>A
NM_000027.3:c.-36G>A NP_000018.2:n.-36G>A
NM_001171988.1:c.-36G>A NP_001165459.1:n.-36G>A
NR_033655.1:n.93G>A
XM_006714123.2:c.-36G>A XP_006714186.1:n.-36G>A
XR_001741155.2:n.59G>A
NM_000027.4:c.-36G>A MANE Select NP_000018.2:n.-36G>A
NM_001171988.2:c.-36G>A NP_001165459.1:n.-36G>A
NR_033655.2:n.27G>A