Canonical Allele Identifier: CA665634085
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1383810310
MyVariant Identifiers: chr10:g.46046437C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046437C>T , CM000672.2:g.46046437C>T GRCh38
NC_000010.10:g.51549385G>A , CM000672.1:g.51549385G>A GRCh37
NC_000010.9:g.51219391G>A NCBI36
NG_011551.1:g.4833G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-58G>A ENSP00000499419.1:n.-142-58G>A
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