Canonical Allele Identifier: CA816329963

Gene: OFCC1

Linked Data

• dbSNP Id: rs1423748183
• gnomAD v3: 6-10175696-G-GC
• gnomAD v4: 6-10175696-G-GC
• MyVariant Identifiers: chr6:g.10175929_10175930insC (hg19) ; chr6:g.10175696_10175697insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10175696_10175697insC , CM000668.2:g.10175696_10175697insC	GRCh38
NC_000006.11:g.10175929_10175930insC , CM000668.1:g.10175929_10175930insC	GRCh37
NC_000006.10:g.10283915_10283916insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462111.1:n.164-16198_164-16197insG
ENST00000481704.1:c.-101-16198_-101-16197insG	ENSP00000418286.1:n.-101-16198_-101-16197insG
XM_017011612.1:c.-101-16198_-101-16197insG	XP_016867101.1:n.-101-16198_-101-16197insG
NR_170155.1:n.232-16198_232-16197insG