Canonical Allele Identifier: CA2086122722
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776775T= , CM000675.2:g.39776775T= GRCh38
NC_000013.10:g.40350912T= , CM000675.1:g.40350912T= GRCh37
NC_000013.9:g.39248912T= NCBI36
NG_028352.1:g.126149T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000416691.5:c.1827-11560T= ENSP00000403733.1:n.1827-11560T=
NM_001145079.1:c.1827-11560T= NP_001138551.1:n.1827-11560T=
NM_001145079.2:c.1827-11560T= NP_001138551.1:n.1827-11560T=