Canonical Allele Identifier: CA10620601
Gene: AGA HGNC NCBI

Linked Data

ClinVar Variation Id: 348239
ClinVar RCV Id: RCV000275104
dbSNP Id: rs886059264
gnomAD v3: 4-177442469-C-T
gnomAD v4: 4-177442469-C-T
MyVariant Identifiers: chr4:g.178363623C>T (hg19) chr4:g.177442469C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442469C>T , CM000666.2:g.177442469C>T GRCh38
NC_000004.11:g.178363623C>T , CM000666.1:g.178363623C>T GRCh37
NC_000004.10:g.178600617C>T NCBI36
NG_011845.2:g.5035G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.6:c.-94G>A ENSP00000264595.2:n.-94G>A
NM_000027.3:c.-94G>A NP_000018.2:n.-94G>A
NM_001171988.1:c.-94G>A NP_001165459.1:n.-94G>A
NR_033655.1:n.35G>A
XM_006714123.2:c.-94G>A XP_006714186.1:n.-94G>A
XR_001741155.2:n.1G>A
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