Canonical Allele Identifier: CA955200498
Gene: COG6 HGNC NCBI

Linked Data

dbSNP Id: rs1881471159

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776612A>G , CM000675.2:g.39776612A>G GRCh38
NC_000013.10:g.40350749A>G , CM000675.1:g.40350749A>G GRCh37
NC_000013.9:g.39248749A>G NCBI36
NG_028352.1:g.125986A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000416691.5:c.1827-11723A>G ENSP00000403733.1:n.1827-11723A>G
NM_001145079.1:c.1827-11723A>G NP_001138551.1:n.1827-11723A>G
NM_001145079.2:c.1827-11723A>G NP_001138551.1:n.1827-11723A>G