Canonical Allele Identifier: CA13220506
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs10993994
gnomAD v2: 10-51549496-T-C
gnomAD v3: 10-46046326-A-G
gnomAD v4: 10-46046326-A-G
MyVariant Identifiers: chr10:g.51549496T>C (hg19) chr10:g.46046326A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046326A>G , CM000672.2:g.46046326A>G GRCh38
NC_000010.10:g.51549496T>C , CM000672.1:g.51549496T>C GRCh37
NC_000010.9:g.51219502T>C NCBI36
NG_011551.1:g.4944T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-89T>C ENSP00000499419.1:n.-89T>C
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