Canonical Allele Identifier: CA206401207

Gene: MSMB

Linked Data

• dbSNP Id: rs201727405
• MyVariant Identifiers: chr10:g.51549219A>G (hg19) ; chr10:g.46046603T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046603T>C , CM000672.2:g.46046603T>C	GRCh38
NC_000010.10:g.51549219A>G , CM000672.1:g.51549219A>G	GRCh37
NC_000010.9:g.51219225A>G	NCBI36
NG_011551.1:g.4667A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-142-224A>G	ENSP00000499419.1:n.-142-224A>G