Canonical Allele Identifier: CA469555239

Gene: MSMB

Linked Data

• dbSNP Id: rs781959829
• gnomAD v2: 10-51549312-T-C
• gnomAD v3: 10-46046510-A-G
• gnomAD v4: 10-46046510-A-G
• MyVariant Identifiers: chr10:g.51549312T>C (hg19) ; chr10:g.46046510A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046510A>G , CM000672.2:g.46046510A>G	GRCh38
NC_000010.10:g.51549312T>C , CM000672.1:g.51549312T>C	GRCh37
NC_000010.9:g.51219318T>C	NCBI36
NG_011551.1:g.4760T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000663171.1:c.-142-131T>C	ENSP00000499419.1:n.-142-131T>C