Canonical Allele Identifier: CA757474932
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1477769716
MyVariant Identifiers: chr2:g.136603198T>C (hg19) chr2:g.135845628T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845628T>C , CM000664.2:g.135845628T>C GRCh38
NC_000002.11:g.136603198T>C , CM000664.1:g.136603198T>C GRCh37
NC_000002.10:g.136319668T>C NCBI36
NG_008104.2:g.14542A>G , LRG_338:g.14542A>G
NG_008958.1:g.35814A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+609A>G MANE Select ENSP00000264156.2:n.2209+609A>G
ENST00000264156.2:c.2209+609A>G ENSP00000264156.2:n.2209+609A>G
ENST00000492091.1:n.635+609A>G
NM_005915.5:c.2209+609A>G NP_005906.2:n.2209+609A>G
NM_005915.6:c.2209+609A>G MANE Select NP_005906.2:n.2209+609A>G
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