Canonical Allele Identifier: CA376628854
Gene: MSMB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.46046349G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046349G>C , CM000672.2:g.46046349G>C GRCh38
NC_000010.10:g.51549473C>G , CM000672.1:g.51549473C>G GRCh37
NC_000010.9:g.51219479C>G NCBI36
NG_011551.1:g.4921C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-112C>G ENSP00000499419.1:n.-112C>G
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