Canonical Allele Identifier: CA1515649850
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs200021845

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442422C>A , CM000666.2:g.177442422C>A GRCh38
NC_000004.11:g.178363576C>A , CM000666.1:g.178363576C>A GRCh37
NC_000004.10:g.178600570C>A NCBI36
NG_011845.2:g.5082G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-47G>T MANE Select ENSP00000264595.2:n.-47G>T
ENST00000264595.6:c.-47G>T ENSP00000264595.2:n.-47G>T
NM_000027.3:c.-47G>T NP_000018.2:n.-47G>T
NM_001171988.1:c.-47G>T NP_001165459.1:n.-47G>T
NR_033655.1:n.82G>T
XM_006714123.2:c.-47G>T XP_006714186.1:n.-47G>T
XR_001741155.2:n.48G>T
NM_000027.4:c.-47G>T MANE Select NP_000018.2:n.-47G>T
NM_001171988.2:c.-47G>T NP_001165459.1:n.-47G>T
NR_033655.2:n.16G>T