Canonical Allele Identifier: CA720945542
Gene: ORC6 HGNC NCBI

Linked Data

dbSNP Id: rs1477460438
MyVariant Identifiers: chr16:g.46732010G>C (hg19) chr16:g.46698098G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698098G>C , CM000678.2:g.46698098G>C GRCh38
NC_000016.9:g.46732010G>C , CM000678.1:g.46732010G>C GRCh37
NC_000016.8:g.45289511G>C NCBI36
NG_028241.1:g.13453G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*513G>C MANE Select ENSP00000219097.2:n.*513G>C
ENST00000219097.6:c.*513G>C ENSP00000219097.2:n.*513G>C
ENST00000566860.1:c.*513G>C ENSP00000456981.1:n.*513G>C
ENST00000567000.2:n.1276G>C
NM_014321.3:c.*513G>C NP_055136.1:n.*513G>C
NR_037620.1:n.1391G>C
NM_014321.4:c.*513G>C MANE Select NP_055136.1:n.*513G>C
NR_037620.2:n.1378G>C
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