Canonical Allele Identifier: CA2086122699
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776724C= , CM000675.2:g.39776724C= GRCh38
NC_000013.10:g.40350861C= , CM000675.1:g.40350861C= GRCh37
NC_000013.9:g.39248861C= NCBI36
NG_028352.1:g.126098C=

Transcript Alleles

HGVS Amino-acid change
ENST00000416691.5:c.1827-11611C= ENSP00000403733.1:n.1827-11611C=
NM_001145079.1:c.1827-11611C= NP_001138551.1:n.1827-11611C=
NM_001145079.2:c.1827-11611C= NP_001138551.1:n.1827-11611C=