Canonical Allele Identifier: CA1290852252
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1679895162

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856525C>A , CM000664.2:g.135856525C>A GRCh38
NC_000002.11:g.136614095C>A , CM000664.1:g.136614095C>A GRCh37
NC_000002.10:g.136330565C>A NCBI36
NG_008104.2:g.3645G>T , LRG_338:g.3645G>T
NG_008958.1:g.24917G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+203G>T MANE Select ENSP00000264156.2:n.1626+203G>T
ENST00000264156.2:c.1626+203G>T ENSP00000264156.2:n.1626+203G>T
ENST00000492091.1:n.182-4962G>T
NM_005915.5:c.1626+203G>T NP_005906.2:n.1626+203G>T
NM_005915.6:c.1626+203G>T MANE Select NP_005906.2:n.1626+203G>T