Canonical Allele Identifier: CA2579834953
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs2132429777
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046625C>T , CM000672.2:g.46046625C>T GRCh38
NC_000010.10:g.51549197G>A , CM000672.1:g.51549197G>A GRCh37
NC_000010.9:g.51219203G>A NCBI36
NG_011551.1:g.4645G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-246G>A ENSP00000499419.1:n.-142-246G>A
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