Canonical Allele Identifier: CA757439708
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1316346472
gnomAD v3: 2-135859108-G-A
gnomAD v4: 2-135859108-G-A
MyVariant Identifiers: chr2:g.136616678G>A (hg19) chr2:g.135859108G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859108G>A , CM000664.2:g.135859108G>A GRCh38
NC_000002.11:g.136616678G>A , CM000664.1:g.136616678G>A GRCh37
NC_000002.10:g.136333148G>A NCBI36
NG_008104.2:g.1062C>T , LRG_338:g.1062C>T
NG_008958.1:g.22334C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+193C>T MANE Select ENSP00000264156.2:n.1362+193C>T
ENST00000264156.2:c.1362+193C>T ENSP00000264156.2:n.1362+193C>T
ENST00000492091.1:n.181+3499C>T
NM_005915.5:c.1362+193C>T NP_005906.2:n.1362+193C>T
NM_005915.6:c.1362+193C>T MANE Select NP_005906.2:n.1362+193C>T
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