Canonical Allele Identifier: CA757474985

Gene: MCM6

Linked Data

• dbSNP Id: rs1274436691
• MyVariant Identifiers: chr2:g.136603237T>A (hg19) ; chr2:g.135845667T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135845667T>A , CM000664.2:g.135845667T>A	GRCh38
NC_000002.11:g.136603237T>A , CM000664.1:g.136603237T>A	GRCh37
NC_000002.10:g.136319707T>A	NCBI36
NG_008104.2:g.14503A>T , LRG_338:g.14503A>T
NG_008958.1:g.35775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264156.3:c.2209+570A>T MANE Select	ENSP00000264156.2:n.2209+570A>T
ENST00000264156.2:c.2209+570A>T	ENSP00000264156.2:n.2209+570A>T
ENST00000492091.1:n.635+570A>T
NM_005915.5:c.2209+570A>T	NP_005906.2:n.2209+570A>T
NM_005915.6:c.2209+570A>T MANE Select	NP_005906.2:n.2209+570A>T