Canonical Allele Identifier: CA469555249
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs540793006
gnomAD v3: 10-46046610-T-C
gnomAD v4: 10-46046610-T-C
MyVariant Identifiers: chr10:g.51549212A>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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