Canonical Allele Identifier: CA56601752
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs4988234

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851103C>T , CM000664.2:g.135851103C>T GRCh38
NC_000002.11:g.136608673C>T , CM000664.1:g.136608673C>T GRCh37
NC_000002.10:g.136325143C>T NCBI36
NG_008104.2:g.9067G>A , LRG_338:g.9067G>A
NG_008958.1:g.30339G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+299G>A MANE Select ENSP00000264156.2:p.=
ENST00000264156.2:c.1917+299G>A ENSP00000264156.2:p.=
ENST00000483902.1:n.544+299G>A
ENST00000492091.1:n.343+299G>A
NM_005915.5:c.1917+299G>A NP_005906.2:p.=
NM_005915.6:c.1917+299G>A MANE Select NP_005906.2:p.=