Canonical Allele Identifier: CA757437938

Gene: MCM6

Linked Data

• dbSNP Id: rs1315941705
• gnomAD v4: 2-135856609-CCT-C
• MyVariant Identifiers: chr2:g.136614180_136614181del (hg19) ; chr2:g.135856610_135856611del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135856610_135856611del , CM000664.2:g.135856610_135856611del	GRCh38
NC_000002.11:g.136614180_136614181del , CM000664.1:g.136614180_136614181del	GRCh37
NC_000002.10:g.136330650_136330651del	NCBI36
NG_008104.2:g.3559_3560del , LRG_338:g.3559_3560del
NG_008958.1:g.24831_24832del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264156.3:c.1626+117_1626+118del MANE Select	ENSP00000264156.2:n.1626+117_1626+118del
ENST00000264156.2:c.1626+117_1626+118del	ENSP00000264156.2:n.1626+117_1626+118del
ENST00000492091.1:n.182-5048_182-5047del
NM_005915.5:c.1626+117_1626+118del	NP_005906.2:n.1626+117_1626+118del
NM_005915.6:c.1626+117_1626+118del MANE Select	NP_005906.2:n.1626+117_1626+118del