Canonical Allele Identifier: CA10654603

Gene: RANBP2

Linked Data

• ClinVar Variation Id: 369306
• ClinVar RCV Id: RCV000376277
• dbSNP Id: rs17037035
• gnomAD v2: 2-109510913-C-T
• gnomAD v3: 2-108894457-C-T
• gnomAD v4: 2-108894457-C-T
• MyVariant Identifiers: chr2:g.109510913C>T (hg19) ; chr2:g.108894457C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108894457C>T , CM000664.2:g.108894457C>T	GRCh38
NC_000002.11:g.109510913C>T , CM000664.1:g.109510913C>T	GRCh37
NC_000002.10:g.108877345C>T	NCBI36
NG_008257.1:g.99916G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_017004623.2:c.8370+121411C>T	XP_016860112.1:n.8370+121411C>T