Canonical Allele Identifier: CA757437937
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1196851266
gnomAD v4: 2-135856597-A-T
MyVariant Identifiers: chr2:g.136614167A>T (hg19) chr2:g.135856597A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856597A>T , CM000664.2:g.135856597A>T GRCh38
NC_000002.11:g.136614167A>T , CM000664.1:g.136614167A>T GRCh37
NC_000002.10:g.136330637A>T NCBI36
NG_008104.2:g.3573T>A , LRG_338:g.3573T>A
NG_008958.1:g.24845T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+131T>A MANE Select ENSP00000264156.2:n.1626+131T>A
ENST00000264156.2:c.1626+131T>A ENSP00000264156.2:n.1626+131T>A
ENST00000492091.1:n.182-5034T>A
NM_005915.5:c.1626+131T>A NP_005906.2:n.1626+131T>A
NM_005915.6:c.1626+131T>A MANE Select NP_005906.2:n.1626+131T>A
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