Canonical Allele Identifier: CA442332831
Gene: AGA HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.178360803T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439649T>C , CM000666.2:g.177439649T>C GRCh38
NC_000004.11:g.178360803T>C , CM000666.1:g.178360803T>C GRCh37
NC_000004.10:g.178597797T>C NCBI36
NG_011845.2:g.7855A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.321A>G MANE Select ENSP00000264595.2:p.Arg107=
ENST00000264595.6:c.321A>G ENSP00000264595.2:p.Arg107=
ENST00000506853.5:n.355A>G
ENST00000510635.1:c.17A>G
ENST00000510955.5:n.315+624A>G
NM_000027.3:c.321A>G NP_000018.2:p.Arg107=
NM_001171988.1:c.321A>G NP_001165459.1:p.Arg107=
NR_033655.1:n.449A>G
XM_006714123.2:c.321A>G XP_006714186.1:p.Arg107=
XR_001741155.2:n.415A>G
NM_000027.4:c.321A>G MANE Select NP_000018.2:p.Arg107=
NM_001171988.2:c.321A>G NP_001165459.1:p.Arg107=
NR_033655.2:n.383A>G