Canonical Allele Identifier: CA56601662
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs866925781
MyVariant Identifiers: chr2:g.136608601T>C (hg19) chr2:g.135851031T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851031T>C , CM000664.2:g.135851031T>C GRCh38
NC_000002.11:g.136608601T>C , CM000664.1:g.136608601T>C GRCh37
NC_000002.10:g.136325071T>C NCBI36
NG_008104.2:g.9139A>G , LRG_338:g.9139A>G
NG_008958.1:g.30411A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1917+371A>G MANE Select ENSP00000264156.2:n.1917+371A>G
ENST00000264156.2:c.1917+371A>G ENSP00000264156.2:n.1917+371A>G
ENST00000483902.1:n.544+371A>G
ENST00000492091.1:n.343+371A>G
NM_005915.5:c.1917+371A>G NP_005906.2:n.1917+371A>G
NM_005915.6:c.1917+371A>G MANE Select NP_005906.2:n.1917+371A>G
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