Canonical Allele Identifier: CA1290849730

Gene: MCM6

Linked Data

• dbSNP Id: rs1679773673

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135851159T>C , CM000664.2:g.135851159T>C	GRCh38
NC_000002.11:g.136608729T>C , CM000664.1:g.136608729T>C	GRCh37
NC_000002.10:g.136325199T>C	NCBI36
NG_008104.2:g.9011A>G , LRG_338:g.9011A>G
NG_008958.1:g.30283A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264156.3:c.1917+243A>G MANE Select	ENSP00000264156.2:n.1917+243A>G
ENST00000264156.2:c.1917+243A>G	ENSP00000264156.2:n.1917+243A>G
ENST00000483902.1:n.544+243A>G
ENST00000492091.1:n.343+243A>G
NM_005915.5:c.1917+243A>G	NP_005906.2:n.1917+243A>G
NM_005915.6:c.1917+243A>G MANE Select	NP_005906.2:n.1917+243A>G