Canonical Allele Identifier: CA10669082
Gene: MYCL HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.39896394C>A
GRCh37 chr1:g.40362066C>A
gnomAD v2:
1:40362066 C / A
gnomAD v3:
1:39896394 C / A
gnomAD v4:
chr1-39896394-C-A
Joint Max Group AF 0.23076524 (NFE)
Genomes Max Group AF 0.23173582 (NFE)
Exomes Max Group AF 0.22552143 (NFE)
dbSNP:
3134615
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39896394C>A , CM000663.2:g.39896394C>A GRCh38
NC_000001.10:g.40362066C>A , CM000663.1:g.40362066C>A GRCh37
NC_000001.9:g.40134653C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397332.3:c.*978G>T ENSP00000380494.2:n.*978G>T
ENST00000372816.3:c.*978G>T MANE Select ENSP00000361903.2:n.*978G>T
ENST00000397332.2:c.*978G>T ENSP00000380494.2:n.*978G>T
NM_001033081.2:c.*978G>T NP_001028253.1:n.*978G>T
NM_001033082.2:c.*978G>T NP_001028254.2:n.*978G>T
NM_001033081.3:c.*978G>T MANE Select NP_001028253.1:n.*978G>T
NM_001033082.3:c.*978G>T NP_001028254.2:n.*978G>T
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