Canonical Allele Identifier: CA665634027

Gene: MSMB

Linked Data

• dbSNP Id: rs1422798045
• gnomAD v4: 10-46046359-T-G
• MyVariant Identifiers: chr10:g.46046359T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046359T>G , CM000672.2:g.46046359T>G	GRCh38
NC_000010.10:g.51549463A>C , CM000672.1:g.51549463A>C	GRCh37
NC_000010.9:g.51219469A>C	NCBI36
NG_011551.1:g.4911A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-122A>C	ENSP00000499419.1:n.-122A>C