Canonical Allele Identifier: CA2672747108
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs1736855705

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437331G>A , CM000666.2:g.177437331G>A GRCh38
NC_000004.11:g.178358485G>A , CM000666.1:g.178358485G>A GRCh37
NC_000004.10:g.178595479G>A NCBI36
NG_011845.2:g.10173C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.622+74C>T MANE Select ENSP00000264595.2:n.622+74C>T
ENST00000264595.6:c.622+74C>T ENSP00000264595.2:n.622+74C>T
ENST00000502310.5:c.277+74C>T ENSP00000423798.1:n.277+74C>T
ENST00000506853.5:n.656+74C>T
ENST00000510635.1:c.318+74C>T
ENST00000510955.5:n.617C>T
NM_000027.3:c.622+74C>T NP_000018.2:n.622+74C>T
NM_001171988.1:c.622+74C>T NP_001165459.1:n.622+74C>T
NR_033655.1:n.750+74C>T
XM_006714123.2:c.622+74C>T XP_006714186.1:n.622+74C>T
XR_001741155.2:n.716+74C>T
NM_000027.4:c.622+74C>T MANE Select NP_000018.2:n.622+74C>T
NM_001171988.2:c.622+74C>T NP_001165459.1:n.622+74C>T
NR_033655.2:n.684+74C>T