Canonical Allele Identifier: CA536398729
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1334602397
gnomAD v2: 2-136603222-A-C
gnomAD v3: 2-135845652-A-C
gnomAD v4: 2-135845652-A-C
MyVariant Identifiers: chr2:g.136603222A>C (hg19) chr2:g.135845652A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845652A>C , CM000664.2:g.135845652A>C GRCh38
NC_000002.11:g.136603222A>C , CM000664.1:g.136603222A>C GRCh37
NC_000002.10:g.136319692A>C NCBI36
NG_008104.2:g.14518T>G , LRG_338:g.14518T>G
NG_008958.1:g.35790T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+585T>G MANE Select ENSP00000264156.2:n.2209+585T>G
ENST00000264156.2:c.2209+585T>G ENSP00000264156.2:n.2209+585T>G
ENST00000492091.1:n.635+585T>G
NM_005915.5:c.2209+585T>G NP_005906.2:n.2209+585T>G
NM_005915.6:c.2209+585T>G MANE Select NP_005906.2:n.2209+585T>G
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