Canonical Allele Identifier: CA2086122709
Gene: COG6 HGNC NCBI

Linked Data

dbSNP Id: rs1881475953

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776744G>C , CM000675.2:g.39776744G>C GRCh38
NC_000013.10:g.40350881G>C , CM000675.1:g.40350881G>C GRCh37
NC_000013.9:g.39248881G>C NCBI36
NG_028352.1:g.126118G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000416691.5:c.1827-11591G>C ENSP00000403733.1:n.1827-11591G>C
NM_001145079.1:c.1827-11591G>C NP_001138551.1:n.1827-11591G>C
NM_001145079.2:c.1827-11591G>C NP_001138551.1:n.1827-11591G>C