Canonical Allele Identifier: CA593320518
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1475686386
gnomAD v2: 10-51549448-C-G
gnomAD v3: 10-46046374-G-C
gnomAD v4: 10-46046374-G-C
MyVariant Identifiers: chr10:g.51549448C>G (hg19) chr10:g.46046374G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046374G>C , CM000672.2:g.46046374G>C GRCh38
NC_000010.10:g.51549448C>G , CM000672.1:g.51549448C>G GRCh37
NC_000010.9:g.51219454C>G NCBI36
NG_011551.1:g.4896C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-137C>G ENSP00000499419.1:n.-137C>G
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