Canonical Allele Identifier: CA440520129
Gene: CISD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 506867
ClinVar RCV Id: RCV000604966
dbSNP Id: rs1553968629
gnomAD v4: 4-102869053-G-A
MyVariant Identifiers: chr4:g.103790210G>A (hg19) chr4:g.102869053G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102869053G>A , CM000666.2:g.102869053G>A GRCh38
NC_000004.11:g.103790210G>A , CM000666.1:g.103790210G>A GRCh37
NC_000004.10:g.104009651G>A NCBI36
NG_008636.2:g.5076G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000273986.10:c.-32G>A MANE Select ENSP00000273986.4:n.-32G>A
ENST00000646632.1:c.-32G>A ENSP00000494257.1:n.-32G>A
ENST00000273986.8:c.-32G>A ENSP00000273986.4:n.-32G>A
NM_001008388.4:c.-32G>A NP_001008389.1:n.-32G>A
NM_001008388.5:c.-32G>A MANE Select NP_001008389.1:n.-32G>A
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