Canonical Allele Identifier: CA1888946
Gene: MCM6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs309180

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856685G>A , CM000664.2:g.135856685G>A GRCh38
NC_000002.11:g.136614255G>A , CM000664.1:g.136614255G>A GRCh37
NC_000002.10:g.136330725G>A NCBI36
NG_008104.2:g.3485C>T , LRG_338:g.3485C>T
NG_008958.1:g.24757C>T

Transcript Alleles

HGVS Amino-acid change
NM_005915.5:c.1626+43C>T VV NP_005906.2:p.=
NM_005915.6:c.1626+43C>T VV MANE Preferred
ENST00000264156.2:c.1626+43C>T ENSP00000264156.2:p.=
ENST00000492091.1:n.182-5122C>T