Canonical Allele Identifier: CA206401158
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs780150806
gnomAD v3: 10-46046532-C-T
gnomAD v4: 10-46046532-C-T
MyVariant Identifiers: chr10:g.51549290G>A (hg19) chr10:g.46046532C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046532C>T , CM000672.2:g.46046532C>T GRCh38
NC_000010.10:g.51549290G>A , CM000672.1:g.51549290G>A GRCh37
NC_000010.9:g.51219296G>A NCBI36
NG_011551.1:g.4738G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-153G>A ENSP00000499419.1:n.-142-153G>A
Search 100 bp 5'
Search 100 bp 3'