Canonical Allele Identifier: CA2579834951

Gene: MSMB

Linked Data

• dbSNP Id: rs2132429777

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046625C>G , CM000672.2:g.46046625C>G	GRCh38
NC_000010.10:g.51549197G>C , CM000672.1:g.51549197G>C	GRCh37
NC_000010.9:g.51219203G>C	NCBI36
NG_011551.1:g.4645G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-142-246G>C	ENSP00000499419.1:n.-142-246G>C