Canonical Allele Identifier: CA757475011
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1429685629
gnomAD v3: 2-135845716-TA-T
gnomAD v4: 2-135845716-TA-T
MyVariant Identifiers: chr2:g.136603287del (hg19) chr2:g.135845717del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845720del , CM000664.2:g.135845720del GRCh38
NC_000002.11:g.136603290del , CM000664.1:g.136603290del GRCh37
NC_000002.10:g.136319760del NCBI36
NG_008104.2:g.14453del , LRG_338:g.14453del
NG_008958.1:g.35725del

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.2209+520del MANE Select ENSP00000264156.2:n.2209+520del
ENST00000264156.2:c.2209+520del ENSP00000264156.2:n.2209+520del
ENST00000492091.1:n.635+520del
NM_005915.5:c.2209+520del NP_005906.2:n.2209+520del
NM_005915.6:c.2209+520del MANE Select NP_005906.2:n.2209+520del
Search 100 bp 5'
Search 100 bp 3'