Canonical Allele Identifier: CA1907224371
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1840906585
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046596_46046597insGC , CM000672.2:g.46046596_46046597insGC GRCh38
NC_000010.10:g.51549225_51549226insGC , CM000672.1:g.51549225_51549226insGC GRCh37
NC_000010.9:g.51219231_51219232insGC NCBI36
NG_011551.1:g.4673_4674insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-218_-142-217insGC ENSP00000499419.1:n.-142-218_-142-217insGC
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