Canonical Allele Identifier: CA2581815982
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845706T>G , CM000664.2:g.135845706T>G GRCh38
NC_000002.11:g.136603276T>G , CM000664.1:g.136603276T>G GRCh37
NC_000002.10:g.136319746T>G NCBI36
NG_008104.2:g.14464A>C , LRG_338:g.14464A>C
NG_008958.1:g.35736A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.2209+531A>C MANE Select ENSP00000264156.2:n.2209+531A>C
ENST00000264156.2:c.2209+531A>C ENSP00000264156.2:n.2209+531A>C
ENST00000492091.1:n.635+531A>C
NM_005915.5:c.2209+531A>C NP_005906.2:n.2209+531A>C
NM_005915.6:c.2209+531A>C MANE Select NP_005906.2:n.2209+531A>C