Canonical Allele Identifier: CA10846212
Gene: CYMP HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.110491187T>C
GRCh37 chr1:g.111033809T>C
gnomAD v2:
1:111033809 T / C
gnomAD v3:
1:110491187 T / C
gnomAD v4:
chr1-110491187-T-C
Joint Max Group AF 0.92035107 (AFR)
Genomes Max Group AF 0.92035107 (AFR)
Exomes Max Group AF 0.60248321 (NFE)
dbSNP:
4839431
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110491187T>C , CM000663.2:g.110491187T>C GRCh38
NC_000001.10:g.111033809T>C , CM000663.1:g.111033809T>C GRCh37
NC_000001.9:g.110835332T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000462836.2:n.555T>C
ENST00000420853.1:n.359T>C
ENST00000474680.5:n.1173T>C
NR_003599.2:n.1159T>C
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