Canonical Allele Identifier: CA2579835788
Gene: MSMB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046358T>G , CM000672.2:g.46046358T>G GRCh38
NC_000010.10:g.51549464A>C , CM000672.1:g.51549464A>C GRCh37
NC_000010.9:g.51219470A>C NCBI36
NG_011551.1:g.4912A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-121A>C ENSP00000499419.1:n.-121A>C
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