Canonical Allele Identifier: CA1290847299
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845642A= , CM000664.2:g.135845642A= GRCh38
NC_000002.11:g.136603212A= , CM000664.1:g.136603212A= GRCh37
NC_000002.10:g.136319682A= NCBI36
NG_008104.2:g.14528T= , LRG_338:g.14528T=
NG_008958.1:g.35800T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+595T= MANE Select ENSP00000264156.2:n.2209+595T=
ENST00000264156.2:c.2209+595T= ENSP00000264156.2:n.2209+595T=
ENST00000492091.1:n.635+595T=
NM_005915.5:c.2209+595T= NP_005906.2:n.2209+595T=
NM_005915.6:c.2209+595T= MANE Select NP_005906.2:n.2209+595T=