Canonical Allele Identifier: CA1515649722
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1423100091

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442387G>T , CM000666.2:g.177442387G>T GRCh38
NC_000004.11:g.178363541G>T , CM000666.1:g.178363541G>T GRCh37
NC_000004.10:g.178600535G>T NCBI36
NG_011845.2:g.5117C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-12C>A MANE Select ENSP00000264595.2:n.-12C>A
ENST00000264595.6:c.-12C>A ENSP00000264595.2:n.-12C>A
ENST00000506853.5:n.23C>A
ENST00000510955.5:n.23C>A
ENST00000511231.1:n.23C>A
NM_000027.3:c.-12C>A NP_000018.2:n.-12C>A
NM_001171988.1:c.-12C>A NP_001165459.1:n.-12C>A
NR_033655.1:n.117C>A
XM_006714123.2:c.-12C>A XP_006714186.1:n.-12C>A
XR_001741155.2:n.83C>A
NM_000027.4:c.-12C>A MANE Select NP_000018.2:n.-12C>A
NM_001171988.2:c.-12C>A NP_001165459.1:n.-12C>A
NR_033655.2:n.51C>A