Canonical Allele Identifier: CA757437930

Gene: MCM6

Linked Data

• dbSNP Id: rs1477894171
• gnomAD v3: 2-135856562-CTTTAT-C
• gnomAD v4: 2-135856562-CTTTAT-C
• MyVariant Identifiers: chr2:g.136614133_136614137del (hg19) ; chr2:g.135856563_135856567del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135856566_135856570del , CM000664.2:g.135856566_135856570del	GRCh38
NC_000002.11:g.136614136_136614140del , CM000664.1:g.136614136_136614140del	GRCh37
NC_000002.10:g.136330606_136330610del	NCBI36
NG_008104.2:g.3603_3607del , LRG_338:g.3603_3607del
NG_008958.1:g.24875_24879del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264156.3:c.1626+161_1626+165del MANE Select	ENSP00000264156.2:n.1626+161_1626+165del
ENST00000264156.2:c.1626+161_1626+165del	ENSP00000264156.2:n.1626+161_1626+165del
ENST00000492091.1:n.182-5004_182-5000del
NM_005915.5:c.1626+161_1626+165del	NP_005906.2:n.1626+161_1626+165del
NM_005915.6:c.1626+161_1626+165del MANE Select	NP_005906.2:n.1626+161_1626+165del