Canonical Allele Identifier: CA376628860
Gene: MSMB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.46046429T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046429T>A , CM000672.2:g.46046429T>A GRCh38
NC_000010.10:g.51549393A>T , CM000672.1:g.51549393A>T GRCh37
NC_000010.9:g.51219399A>T NCBI36
NG_011551.1:g.4841A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-50A>T ENSP00000499419.1:n.-142-50A>T
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