Canonical Allele Identifier: CA8037523
Gene: ORC6 HGNC NCBI

Linked Data

dbSNP Id: rs772134824
ExAC: 16:46731913 G / C
gnomAD v2: 16-46731913-G-C
gnomAD v3: 16-46698001-G-C
gnomAD v4: 16-46698001-G-C
MyVariant Identifiers: chr16:g.46731913G>C (hg19) chr16:g.46698001G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698001G>C , CM000678.2:g.46698001G>C GRCh38
NC_000016.9:g.46731913G>C , CM000678.1:g.46731913G>C GRCh37
NC_000016.8:g.45289414G>C NCBI36
NG_028241.1:g.13356G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*416G>C MANE Select ENSP00000219097.2:n.*416G>C
ENST00000219097.6:c.*416G>C ENSP00000219097.2:n.*416G>C
ENST00000566860.1:c.*416G>C ENSP00000456981.1:n.*416G>C
ENST00000567000.2:n.1179G>C
NM_014321.3:c.*416G>C NP_055136.1:n.*416G>C
NR_037620.1:n.1294G>C
NM_014321.4:c.*416G>C MANE Select NP_055136.1:n.*416G>C
NR_037620.2:n.1281G>C
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