Canonical Allele Identifier: CA442333190
Gene: AGA HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.178363476C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442322C>T , CM000666.2:g.177442322C>T GRCh38
NC_000004.11:g.178363476C>T , CM000666.1:g.178363476C>T GRCh37
NC_000004.10:g.178600470C>T NCBI36
NG_011845.2:g.5182G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.54G>A MANE Select ENSP00000264595.2:p.Gln18=
ENST00000264595.6:c.54G>A ENSP00000264595.2:p.Gln18=
ENST00000506853.5:n.88G>A
ENST00000510955.5:n.88G>A
ENST00000511231.1:n.88G>A
NM_000027.3:c.54G>A NP_000018.2:p.Gln18=
NM_001171988.1:c.54G>A NP_001165459.1:p.Gln18=
NR_033655.1:n.182G>A
XM_006714123.2:c.54G>A XP_006714186.1:p.Gln18=
XR_001741155.2:n.148G>A
NM_000027.4:c.54G>A MANE Select NP_000018.2:p.Gln18=
NM_001171988.2:c.54G>A NP_001165459.1:p.Gln18=
NR_033655.2:n.116G>A