Canonical Allele Identifier: CA348594680
Gene: MCM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136614303T>A (hg19) chr2:g.135856733T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856733T>A , CM000664.2:g.135856733T>A GRCh38
NC_000002.11:g.136614303T>A , CM000664.1:g.136614303T>A GRCh37
NC_000002.10:g.136330773T>A NCBI36
NG_008104.2:g.3437A>T , LRG_338:g.3437A>T
NG_008958.1:g.24709A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1621A>T MANE Select ENSP00000264156.2:p.Asn541Tyr
ENST00000264156.2:c.1621A>T ENSP00000264156.2:p.Asn541Tyr
ENST00000492091.1:n.182-5170A>T
NM_005915.5:c.1621A>T NP_005906.2:p.Asn541Tyr
NM_005915.6:c.1621A>T MANE Select NP_005906.2:p.Asn541Tyr
Search 100 bp 5'
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