Canonical Allele Identifier: CA665634032
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1212982756
gnomAD v3: 10-46046378-G-A
gnomAD v4: 10-46046378-G-A
MyVariant Identifiers: chr10:g.46046378G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046378G>A , CM000672.2:g.46046378G>A GRCh38
NC_000010.10:g.51549444C>T , CM000672.1:g.51549444C>T GRCh37
NC_000010.9:g.51219450C>T NCBI36
NG_011551.1:g.4892C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-141C>T ENSP00000499419.1:n.-141C>T
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