Canonical Allele Identifier: CA2579836069
Gene: MSMB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046448A>C , CM000672.2:g.46046448A>C GRCh38
NC_000010.10:g.51549374T>G , CM000672.1:g.51549374T>G GRCh37
NC_000010.9:g.51219380T>G NCBI36
NG_011551.1:g.4822T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-69T>G ENSP00000499419.1:n.-142-69T>G
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