Canonical Allele Identifier: CA1290849615

Gene: MCM6

Linked Data

• dbSNP Id: rs1679769296

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135850902del , CM000664.2:g.135850902del	GRCh38
NC_000002.11:g.136608472del , CM000664.1:g.136608472del	GRCh37
NC_000002.10:g.136324942del	NCBI36
NG_008104.2:g.9270del , LRG_338:g.9270del
NG_008958.1:g.30542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264156.3:c.1917+502del MANE Select	ENSP00000264156.2:n.1917+502del
ENST00000264156.2:c.1917+502del	ENSP00000264156.2:n.1917+502del
ENST00000483902.1:n.544+502del
ENST00000492091.1:n.343+502del
NM_005915.5:c.1917+502del	NP_005906.2:n.1917+502del
NM_005915.6:c.1917+502del MANE Select	NP_005906.2:n.1917+502del