Canonical Allele Identifier: CA206401125
Gene: MSMB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.46046413A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046413A>T , CM000672.2:g.46046413A>T GRCh38
NC_000010.10:g.51549409T>A , CM000672.1:g.51549409T>A GRCh37
NC_000010.9:g.51219415T>A NCBI36
NG_011551.1:g.4857T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-34T>A ENSP00000499419.1:n.-142-34T>A
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