Canonical Allele Identifier: CA206401198
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs33967509
MyVariant Identifiers: chr10:g.51549222_51549223insCT (hg19) chr10:g.46046599_46046600insAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046599_46046600insAG , CM000672.2:g.46046599_46046600insAG GRCh38
NC_000010.10:g.51549222_51549223insCT , CM000672.1:g.51549222_51549223insCT GRCh37
NC_000010.9:g.51219228_51219229insCT NCBI36
NG_011551.1:g.4670_4671insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-221_-142-220insCT ENSP00000499419.1:n.-142-221_-142-220insCT
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