Canonical Allele Identifier: CA665634106

Gene: MSMB

Linked Data

• dbSNP Id: rs1468422327
• MyVariant Identifiers: chr10:g.46046447_46046448del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046448_46046449del , CM000672.2:g.46046448_46046449del	GRCh38
NC_000010.10:g.51549374_51549375del , CM000672.1:g.51549374_51549375del	GRCh37
NC_000010.9:g.51219380_51219381del	NCBI36
NG_011551.1:g.4822_4823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-142-69_-142-68del	ENSP00000499419.1:n.-142-69_-142-68del