Canonical Allele Identifier: CA1290852272
Gene: MCM6 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856560G= , CM000664.2:g.135856560G= GRCh38
NC_000002.11:g.136614130G= , CM000664.1:g.136614130G= GRCh37
NC_000002.10:g.136330600G= NCBI36
NG_008104.2:g.3610C= , LRG_338:g.3610C=
NG_008958.1:g.24882C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+168C= MANE Select ENSP00000264156.2:n.1626+168C=
ENST00000264156.2:c.1626+168C= ENSP00000264156.2:n.1626+168C=
ENST00000492091.1:n.182-4997C=
NM_005915.5:c.1626+168C= NP_005906.2:n.1626+168C=
NM_005915.6:c.1626+168C= MANE Select NP_005906.2:n.1626+168C=
Search 100 bp 5'
Search 100 bp 3'