Canonical Allele Identifier: CA2086122645
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776607C= , CM000675.2:g.39776607C= GRCh38
NC_000013.10:g.40350744C= , CM000675.1:g.40350744C= GRCh37
NC_000013.9:g.39248744C= NCBI36
NG_028352.1:g.125981C=

Transcript Alleles

HGVS Amino-acid change
ENST00000416691.5:c.1827-11728C= ENSP00000403733.1:n.1827-11728C=
NM_001145079.1:c.1827-11728C= NP_001138551.1:n.1827-11728C=
NM_001145079.2:c.1827-11728C= NP_001138551.1:n.1827-11728C=