Canonical Allele Identifier: CA134766650

Gene: OFCC1

Linked Data

• dbSNP Id: rs763496167
• MyVariant Identifiers: chr6:g.10175902T>G (hg19) ; chr6:g.10175669T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10175669T>G , CM000668.2:g.10175669T>G	GRCh38
NC_000006.11:g.10175902T>G , CM000668.1:g.10175902T>G	GRCh37
NC_000006.10:g.10283888T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462111.1:n.164-16170A>C
ENST00000481704.1:c.-101-16170A>C	ENSP00000418286.1:n.-101-16170A>C
XM_017011612.1:c.-101-16170A>C	XP_016867101.1:n.-101-16170A>C
NR_170155.1:n.232-16170A>C