Canonical Allele Identifier: CA1290852275
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1029942483
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856561A>G , CM000664.2:g.135856561A>G GRCh38
NC_000002.11:g.136614131A>G , CM000664.1:g.136614131A>G GRCh37
NC_000002.10:g.136330601A>G NCBI36
NG_008104.2:g.3609T>C , LRG_338:g.3609T>C
NG_008958.1:g.24881T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+167T>C MANE Select ENSP00000264156.2:n.1626+167T>C
ENST00000264156.2:c.1626+167T>C ENSP00000264156.2:n.1626+167T>C
ENST00000492091.1:n.182-4998T>C
NM_005915.5:c.1626+167T>C NP_005906.2:n.1626+167T>C
NM_005915.6:c.1626+167T>C MANE Select NP_005906.2:n.1626+167T>C
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