Canonical Allele Identifier: CA2086122697
Gene: COG6 HGNC NCBI

Linked Data

dbSNP Id: rs1881474864

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776717G>A , CM000675.2:g.39776717G>A GRCh38
NC_000013.10:g.40350854G>A , CM000675.1:g.40350854G>A GRCh37
NC_000013.9:g.39248854G>A NCBI36
NG_028352.1:g.126091G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000416691.5:c.1827-11618G>A ENSP00000403733.1:n.1827-11618G>A
NM_001145079.1:c.1827-11618G>A NP_001138551.1:n.1827-11618G>A
NM_001145079.2:c.1827-11618G>A NP_001138551.1:n.1827-11618G>A