Canonical Allele Identifier: CA536399751
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1197209604
gnomAD v2: 2-136616717-G-T
gnomAD v3: 2-135859147-G-T
gnomAD v4: 2-135859147-G-T
MyVariant Identifiers: chr2:g.136616717G>T (hg19) chr2:g.135859147G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859147G>T , CM000664.2:g.135859147G>T GRCh38
NC_000002.11:g.136616717G>T , CM000664.1:g.136616717G>T GRCh37
NC_000002.10:g.136333187G>T NCBI36
NG_008104.2:g.1023C>A , LRG_338:g.1023C>A
NG_008958.1:g.22295C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+154C>A MANE Select ENSP00000264156.2:n.1362+154C>A
ENST00000264156.2:c.1362+154C>A ENSP00000264156.2:n.1362+154C>A
ENST00000492091.1:n.181+3460C>A
NM_005915.5:c.1362+154C>A NP_005906.2:n.1362+154C>A
NM_005915.6:c.1362+154C>A MANE Select NP_005906.2:n.1362+154C>A
Search 100 bp 5'
Search 100 bp 3'