Canonical Allele Identifier: CA1907224220

Gene: MSMB

Linked Data

• dbSNP Id: rs1840901518

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046431A>G , CM000672.2:g.46046431A>G	GRCh38
NC_000010.10:g.51549391T>C , CM000672.1:g.51549391T>C	GRCh37
NC_000010.9:g.51219397T>C	NCBI36
NG_011551.1:g.4839T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000663171.1:c.-142-52T>C	ENSP00000499419.1:n.-142-52T>C