Canonical Allele Identifier: CA348594663

Gene: MCM6

Linked Data

• MyVariant Identifiers: chr2:g.136614296A>G (hg19) ; chr2:g.135856726A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135856726A>G , CM000664.2:g.135856726A>G	GRCh38
NC_000002.11:g.136614296A>G , CM000664.1:g.136614296A>G	GRCh37
NC_000002.10:g.136330766A>G	NCBI36
NG_008104.2:g.3444T>C , LRG_338:g.3444T>C
NG_008958.1:g.24716T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264156.3:c.1626+2T>C MANE Select	ENSP00000264156.2:n.1626+2T>C
ENST00000264156.2:c.1626+2T>C	ENSP00000264156.2:n.1626+2T>C
ENST00000492091.1:n.182-5163T>C
NM_005915.5:c.1626+2T>C	NP_005906.2:n.1626+2T>C
NM_005915.6:c.1626+2T>C MANE Select	NP_005906.2:n.1626+2T>C