Canonical Allele Identifier: CA556485674
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1482793025

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442423G>A , CM000666.2:g.177442423G>A GRCh38
NC_000004.11:g.178363577G>A , CM000666.1:g.178363577G>A GRCh37
NC_000004.10:g.178600571G>A NCBI36
NG_011845.2:g.5081C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-48C>T MANE Select ENSP00000264595.2:n.-48C>T
ENST00000264595.6:c.-48C>T ENSP00000264595.2:n.-48C>T
NM_000027.3:c.-48C>T NP_000018.2:n.-48C>T
NM_001171988.1:c.-48C>T NP_001165459.1:n.-48C>T
NR_033655.1:n.81C>T
XM_006714123.2:c.-48C>T XP_006714186.1:n.-48C>T
XR_001741155.2:n.47C>T
NM_000027.4:c.-48C>T MANE Select NP_000018.2:n.-48C>T
NM_001171988.2:c.-48C>T NP_001165459.1:n.-48C>T
NR_033655.2:n.15C>T