Canonical Allele Identifier: CA2086122669
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776666T= , CM000675.2:g.39776666T= GRCh38
NC_000013.10:g.40350803T= , CM000675.1:g.40350803T= GRCh37
NC_000013.9:g.39248803T= NCBI36
NG_028352.1:g.126040T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000416691.5:c.1827-11669T= ENSP00000403733.1:n.1827-11669T=
NM_001145079.1:c.1827-11669T= NP_001138551.1:n.1827-11669T=
NM_001145079.2:c.1827-11669T= NP_001138551.1:n.1827-11669T=