Canonical Allele Identifier: CA2086122698
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776720T= , CM000675.2:g.39776720T= GRCh38
NC_000013.10:g.40350857T= , CM000675.1:g.40350857T= GRCh37
NC_000013.9:g.39248857T= NCBI36
NG_028352.1:g.126094T=

Transcript Alleles

HGVS Amino-acid change
ENST00000416691.5:c.1827-11615T= ENSP00000403733.1:n.1827-11615T=
NM_001145079.1:c.1827-11615T= NP_001138551.1:n.1827-11615T=
NM_001145079.2:c.1827-11615T= NP_001138551.1:n.1827-11615T=