Canonical Allele Identifier: CA56607356
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs565725105
gnomAD v2: 2-136616718-CT-C
gnomAD v3: 2-135859148-CT-C
gnomAD v4: 2-135859148-CT-C
MyVariant Identifiers: chr2:g.136616719del (hg19) chr2:g.135859149del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859150del , CM000664.2:g.135859150del GRCh38
NC_000002.11:g.136616720del , CM000664.1:g.136616720del GRCh37
NC_000002.10:g.136333190del NCBI36
NG_008104.2:g.1021del , LRG_338:g.1021del
NG_008958.1:g.22293del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+152del MANE Select ENSP00000264156.2:n.1362+152del
ENST00000264156.2:c.1362+152del ENSP00000264156.2:n.1362+152del
ENST00000492091.1:n.181+3458del
NM_005915.5:c.1362+152del NP_005906.2:n.1362+152del
NM_005915.6:c.1362+152del MANE Select NP_005906.2:n.1362+152del
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