Canonical Allele Identifier: CA757474937
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1197274758
MyVariant Identifiers: chr2:g.136603214C>T (hg19) chr2:g.135845644C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845644C>T , CM000664.2:g.135845644C>T GRCh38
NC_000002.11:g.136603214C>T , CM000664.1:g.136603214C>T GRCh37
NC_000002.10:g.136319684C>T NCBI36
NG_008104.2:g.14526G>A , LRG_338:g.14526G>A
NG_008958.1:g.35798G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+593G>A MANE Select ENSP00000264156.2:n.2209+593G>A
ENST00000264156.2:c.2209+593G>A ENSP00000264156.2:n.2209+593G>A
ENST00000492091.1:n.635+593G>A
NM_005915.5:c.2209+593G>A NP_005906.2:n.2209+593G>A
NM_005915.6:c.2209+593G>A MANE Select NP_005906.2:n.2209+593G>A
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