Canonical Allele Identifier: CA206401132
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs910030963
gnomAD v2: 10-51549351-G-A
gnomAD v3: 10-46046471-C-T
gnomAD v4: 10-46046471-C-T
MyVariant Identifiers: chr10:g.51549351G>A (hg19) chr10:g.46046471C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046471C>T , CM000672.2:g.46046471C>T GRCh38
NC_000010.10:g.51549351G>A , CM000672.1:g.51549351G>A GRCh37
NC_000010.9:g.51219357G>A NCBI36
NG_011551.1:g.4799G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-92G>A ENSP00000499419.1:n.-142-92G>A
Search 100 bp 5'
Search 100 bp 3'