Canonical Allele Identifier: CA134766642

Gene: OFCC1

Linked Data

• dbSNP Id: rs561910372
• gnomAD v2: 6-10175833-AGG-A
• gnomAD v3: 6-10175600-AGG-A
• gnomAD v4: 6-10175600-AGG-A
• MyVariant Identifiers: chr6:g.10175834_10175835del (hg19) ; chr6:g.10175601_10175602del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10175601_10175602del , CM000668.2:g.10175601_10175602del	GRCh38
NC_000006.11:g.10175834_10175835del , CM000668.1:g.10175834_10175835del	GRCh37
NC_000006.10:g.10283820_10283821del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462111.1:n.164-16103_164-16102del
ENST00000481704.1:c.-101-16103_-101-16102del	ENSP00000418286.1:n.-101-16103_-101-16102del
XM_017011612.1:c.-101-16103_-101-16102del	XP_016867101.1:n.-101-16103_-101-16102del
NR_170155.1:n.232-16103_232-16102del