Canonical Allele Identifier: CA56601631
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs866523809
MyVariant Identifiers: chr2:g.136608585A>T (hg19) chr2:g.135851015A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851015A>T , CM000664.2:g.135851015A>T GRCh38
NC_000002.11:g.136608585A>T , CM000664.1:g.136608585A>T GRCh37
NC_000002.10:g.136325055A>T NCBI36
NG_008104.2:g.9155T>A , LRG_338:g.9155T>A
NG_008958.1:g.30427T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+387T>A MANE Select ENSP00000264156.2:n.1917+387T>A
ENST00000264156.2:c.1917+387T>A ENSP00000264156.2:n.1917+387T>A
ENST00000483902.1:n.544+387T>A
ENST00000492091.1:n.343+387T>A
NM_005915.5:c.1917+387T>A NP_005906.2:n.1917+387T>A
NM_005915.6:c.1917+387T>A MANE Select NP_005906.2:n.1917+387T>A
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