Canonical Allele Identifier: CA1907224107

Gene: MSMB

Linked Data

• dbSNP Id: rs1590200664

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046344A>G , CM000672.2:g.46046344A>G	GRCh38
NC_000010.10:g.51549478T>C , CM000672.1:g.51549478T>C	GRCh37
NC_000010.9:g.51219484T>C	NCBI36
NG_011551.1:g.4926T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-107T>C	ENSP00000499419.1:n.-107T>C