Canonical Allele Identifier: CA1290847330
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1575357618

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845700G>A , CM000664.2:g.135845700G>A GRCh38
NC_000002.11:g.136603270G>A , CM000664.1:g.136603270G>A GRCh37
NC_000002.10:g.136319740G>A NCBI36
NG_008104.2:g.14470C>T , LRG_338:g.14470C>T
NG_008958.1:g.35742C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+537C>T MANE Select ENSP00000264156.2:n.2209+537C>T
ENST00000264156.2:c.2209+537C>T ENSP00000264156.2:n.2209+537C>T
ENST00000492091.1:n.635+537C>T
NM_005915.5:c.2209+537C>T NP_005906.2:n.2209+537C>T
NM_005915.6:c.2209+537C>T MANE Select NP_005906.2:n.2209+537C>T