Canonical Allele Identifier: CA14488113

Gene: CASC17

Linked Data

• dbSNP Id: rs11654749
• gnomAD v2: 17-69125606-G-T
• gnomAD v3: 17-71129465-G-T
• gnomAD v4: 17-71129465-G-T
• MyVariant Identifiers: chr17:g.69125606G>T (hg19) ; chr17:g.71129465G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71129465G>T , CM000679.2:g.71129465G>T	GRCh38
NC_000017.10:g.69125606G>T , CM000679.1:g.69125606G>T	GRCh37
NC_000017.9:g.66637201G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104152.1:n.217+2925C>A