Canonical Allele Identifier: CA442332294
Gene: AGA HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.178355583T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434429T>C , CM000666.2:g.177434429T>C GRCh38
NC_000004.11:g.178355583T>C , CM000666.1:g.178355583T>C GRCh37
NC_000004.10:g.178592577T>C NCBI36
NG_011845.2:g.13075A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.759A>G MANE Select ENSP00000264595.2:p.Ala253=
ENST00000264595.6:c.759A>G ENSP00000264595.2:p.Ala253=
ENST00000502310.5:c.330A>G ENSP00000423798.1:p.Ala110=
ENST00000506853.5:n.717A>G
NM_000027.3:c.759A>G NP_000018.2:p.Ala253=
NM_001171988.1:c.729A>G NP_001165459.1:p.Ala243=
NR_033655.1:n.811A>G
XM_006714123.2:c.*53A>G XP_006714186.1:n.*53A>G
XR_001741155.2:n.831A>G
NM_000027.4:c.759A>G MANE Select NP_000018.2:p.Ala253=
NM_001171988.2:c.729A>G NP_001165459.1:p.Ala243=
NR_033655.2:n.745A>G