Canonical Allele Identifier: CA1290852309
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856615G= , CM000664.2:g.135856615G= GRCh38
NC_000002.11:g.136614185G= , CM000664.1:g.136614185G= GRCh37
NC_000002.10:g.136330655G= NCBI36
NG_008104.2:g.3555C= , LRG_338:g.3555C=
NG_008958.1:g.24827C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626+113C= MANE Select ENSP00000264156.2:n.1626+113C=
ENST00000264156.2:c.1626+113C= ENSP00000264156.2:n.1626+113C=
ENST00000492091.1:n.182-5052C=
NM_005915.5:c.1626+113C= NP_005906.2:n.1626+113C=
NM_005915.6:c.1626+113C= MANE Select NP_005906.2:n.1626+113C=