Canonical Allele Identifier: CA206401082
Gene: MSMB HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.46046289A>C
GRCh37 chr10:g.51549533T>G
gnomAD v2:
10:51549533 T / G
gnomAD v3:
10:46046289 A / C
gnomAD v4:
chr10-46046289-A-C
Joint Max Group AF 0.01267132 (NFE)
Genomes Max Group AF 0.01143996 (NFE)
Exomes Max Group AF 0.01271068 (NFE)
dbSNP:
41274660
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046289A>C , CM000672.2:g.46046289A>C GRCh38
NC_000010.10:g.51549533T>G , CM000672.1:g.51549533T>G GRCh37
NC_000010.9:g.51219539T>G NCBI36
NG_011551.1:g.4981T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-52T>G ENSP00000499419.1:n.-52T>G
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