Canonical Allele Identifier: CA1036814647
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1679896593
gnomAD v3: 2-135856612-G-A
gnomAD v4: 2-135856612-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856612G>A , CM000664.2:g.135856612G>A GRCh38
NC_000002.11:g.136614182G>A , CM000664.1:g.136614182G>A GRCh37
NC_000002.10:g.136330652G>A NCBI36
NG_008104.2:g.3558C>T , LRG_338:g.3558C>T
NG_008958.1:g.24830C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+116C>T MANE Select ENSP00000264156.2:n.1626+116C>T
ENST00000264156.2:c.1626+116C>T ENSP00000264156.2:n.1626+116C>T
ENST00000492091.1:n.182-5049C>T
NM_005915.5:c.1626+116C>T NP_005906.2:n.1626+116C>T
NM_005915.6:c.1626+116C>T MANE Select NP_005906.2:n.1626+116C>T
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