Canonical Allele Identifier: CA10801547
Gene: MICOS10 HGNC NCBI
COSMIC:
COSN6436847 (not active)
MyVariant.info:
GRCh38 chr1:g.19534612A>G
GRCh37 chr1:g.19861106A>G
gnomAD v2:
1:19861106 A / G
gnomAD v3:
1:19534612 A / G
gnomAD v4:
chr1-19534612-A-G
Joint Max Group AF 0.4749932 (NFE)
Genomes Max Group AF 0.4749932 (NFE)
dbSNP:
10917477
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19534612A>G , CM000663.2:g.19534612A>G GRCh38
NC_000001.10:g.19861106A>G , CM000663.1:g.19861106A>G GRCh37
NC_000001.9:g.19733693A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648702.1:c.-54+49957A>G ENSP00000497006.1:n.-54+49957A>G
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