Canonical Allele Identifier: CA123827
Gene: MSMB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.51549496T>T (hg19)
PubMed: PMID:18264096 PMID:18264097 PMID:19153072 PMID:19383797 PMID:19644707
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046326A= , CM000672.2:g.46046326A= GRCh38
NC_000010.10:g.51549496T= , CM000672.1:g.51549496T= GRCh37
NC_000010.9:g.51219502T= NCBI36
NG_011551.1:g.4944T=

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-89T= ENSP00000499419.1:n.-89T=
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