Canonical Allele Identifier: CA56605771
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs941770393

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856628T>C , CM000664.2:g.135856628T>C GRCh38
NC_000002.11:g.136614198T>C , CM000664.1:g.136614198T>C GRCh37
NC_000002.10:g.136330668T>C NCBI36
NG_008104.2:g.3542A>G , LRG_338:g.3542A>G
NG_008958.1:g.24814A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626+100A>G MANE Select ENSP00000264156.2:n.1626+100A>G
ENST00000264156.2:c.1626+100A>G ENSP00000264156.2:n.1626+100A>G
ENST00000492091.1:n.182-5065A>G
NM_005915.5:c.1626+100A>G NP_005906.2:n.1626+100A>G
NM_005915.6:c.1626+100A>G MANE Select NP_005906.2:n.1626+100A>G