Canonical Allele Identifier: CA593320523

Gene: MSMB

Linked Data

• dbSNP Id: rs1375743974
• gnomAD v2: 10-51549257-T-A
• gnomAD v3: 10-46046565-A-T
• gnomAD v4: 10-46046565-A-T
• MyVariant Identifiers: chr10:g.51549257T>A (hg19) ; chr10:g.46046565A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046565A>T , CM000672.2:g.46046565A>T	GRCh38
NC_000010.10:g.51549257T>A , CM000672.1:g.51549257T>A	GRCh37
NC_000010.9:g.51219263T>A	NCBI36
NG_011551.1:g.4705T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000663171.1:c.-142-186T>A	ENSP00000499419.1:n.-142-186T>A