Canonical Allele Identifier: CA56605711
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs964347926
gnomAD v2: 2-136614100-A-T
gnomAD v3: 2-135856530-A-T
gnomAD v4: 2-135856530-A-T
MyVariant Identifiers: chr2:g.136614100A>T (hg19) chr2:g.135856530A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856530A>T , CM000664.2:g.135856530A>T GRCh38
NC_000002.11:g.136614100A>T , CM000664.1:g.136614100A>T GRCh37
NC_000002.10:g.136330570A>T NCBI36
NG_008104.2:g.3640T>A , LRG_338:g.3640T>A
NG_008958.1:g.24912T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+198T>A MANE Select ENSP00000264156.2:n.1626+198T>A
ENST00000264156.2:c.1626+198T>A ENSP00000264156.2:n.1626+198T>A
ENST00000492091.1:n.182-4967T>A
NM_005915.5:c.1626+198T>A NP_005906.2:n.1626+198T>A
NM_005915.6:c.1626+198T>A MANE Select NP_005906.2:n.1626+198T>A
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