Canonical Allele Identifier: CA2633002598

Gene: ORC6

Linked Data

• gnomAD v4: 16-46698074-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46698074C>T , CM000678.2:g.46698074C>T	GRCh38
NC_000016.9:g.46731986C>T , CM000678.1:g.46731986C>T	GRCh37
NC_000016.8:g.45289487C>T	NCBI36
NG_028241.1:g.13429C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219097.7:c.*489C>T MANE Select	ENSP00000219097.2:n.*489C>T
ENST00000219097.6:c.*489C>T	ENSP00000219097.2:n.*489C>T
ENST00000566860.1:c.*489C>T	ENSP00000456981.1:n.*489C>T
ENST00000567000.2:n.1252C>T
NM_014321.3:c.*489C>T	NP_055136.1:n.*489C>T
NR_037620.1:n.1367C>T
NM_014321.4:c.*489C>T MANE Select	NP_055136.1:n.*489C>T
NR_037620.2:n.1354C>T