Canonical Allele Identifier: CA2700691992
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs2105581248
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856528G>T , CM000664.2:g.135856528G>T GRCh38
NC_000002.11:g.136614098G>T , CM000664.1:g.136614098G>T GRCh37
NC_000002.10:g.136330568G>T NCBI36
NG_008104.2:g.3642C>A , LRG_338:g.3642C>A
NG_008958.1:g.24914C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626+200C>A MANE Select ENSP00000264156.2:n.1626+200C>A
ENST00000264156.2:c.1626+200C>A ENSP00000264156.2:n.1626+200C>A
ENST00000492091.1:n.182-4965C>A
NM_005915.5:c.1626+200C>A NP_005906.2:n.1626+200C>A
NM_005915.6:c.1626+200C>A MANE Select NP_005906.2:n.1626+200C>A
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