Canonical Allele Identifier: CA206401194

Gene: MSMB

Linked Data

• MyVariant Identifiers: chr10:g.51549223_51549224insAG (hg19) ; chr10:g.46046598_46046599insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046598_46046599insCT , CM000672.2:g.46046598_46046599insCT	GRCh38
NC_000010.10:g.51549223_51549224insAG , CM000672.1:g.51549223_51549224insAG	GRCh37
NC_000010.9:g.51219229_51219230insAG	NCBI36
NG_011551.1:g.4671_4672insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-142-220_-142-219insAG	ENSP00000499419.1:n.-142-220_-142-219insAG