Canonical Allele Identifier: CA134766648

Gene: OFCC1

Linked Data

• dbSNP Id: rs946949270
• MyVariant Identifiers: chr6:g.10175891A>T (hg19) ; chr6:g.10175658A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10175658A>T , CM000668.2:g.10175658A>T	GRCh38
NC_000006.11:g.10175891A>T , CM000668.1:g.10175891A>T	GRCh37
NC_000006.10:g.10283877A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462111.1:n.164-16159T>A
ENST00000481704.1:c.-101-16159T>A	ENSP00000418286.1:n.-101-16159T>A
XM_017011612.1:c.-101-16159T>A	XP_016867101.1:n.-101-16159T>A
NR_170155.1:n.232-16159T>A