Canonical Allele Identifier: CA206401239
Gene: MSMB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.46046610T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046610T>G , CM000672.2:g.46046610T>G GRCh38
NC_000010.10:g.51549212A>C , CM000672.1:g.51549212A>C GRCh37
NC_000010.9:g.51219218A>C NCBI36
NG_011551.1:g.4660A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-231A>C ENSP00000499419.1:n.-142-231A>C
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