Canonical Allele Identifier: CA13190090

Gene: MSMB

Linked Data

• dbSNP Id: rs12770171
• gnomAD v2: 10-51549314-C-T
• gnomAD v3: 10-46046508-G-A
• gnomAD v4: 10-46046508-G-A
• MyVariant Identifiers: chr10:g.51549314C>T (hg19) ; chr10:g.46046508G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46046508G>A , CM000672.2:g.46046508G>A	GRCh38
NC_000010.10:g.51549314C>T , CM000672.1:g.51549314C>T	GRCh37
NC_000010.9:g.51219320C>T	NCBI36
NG_011551.1:g.4762C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000663171.1:c.-142-129C>T	ENSP00000499419.1:n.-142-129C>T