Canonical Allele Identifier: CA134766654

Gene: OFCC1

Linked Data

• dbSNP Id: rs767245998
• MyVariant Identifiers: chr6:g.10175955G>C (hg19) ; chr6:g.10175722G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10175722G>C , CM000668.2:g.10175722G>C	GRCh38
NC_000006.11:g.10175955G>C , CM000668.1:g.10175955G>C	GRCh37
NC_000006.10:g.10283941G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462111.1:n.164-16223C>G
ENST00000481704.1:c.-101-16223C>G	ENSP00000418286.1:n.-101-16223C>G
XM_017011612.1:c.-101-16223C>G	XP_016867101.1:n.-101-16223C>G
NR_170155.1:n.232-16223C>G