Canonical Allele Identifier: CA757474933
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1376972356
MyVariant Identifiers: chr2:g.136603202A>T (hg19) chr2:g.135845632A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845632A>T , CM000664.2:g.135845632A>T GRCh38
NC_000002.11:g.136603202A>T , CM000664.1:g.136603202A>T GRCh37
NC_000002.10:g.136319672A>T NCBI36
NG_008104.2:g.14538T>A , LRG_338:g.14538T>A
NG_008958.1:g.35810T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+605T>A MANE Select ENSP00000264156.2:n.2209+605T>A
ENST00000264156.2:c.2209+605T>A ENSP00000264156.2:n.2209+605T>A
ENST00000492091.1:n.635+605T>A
NM_005915.5:c.2209+605T>A NP_005906.2:n.2209+605T>A
NM_005915.6:c.2209+605T>A MANE Select NP_005906.2:n.2209+605T>A
Search 100 bp 5'
Search 100 bp 3'