Canonical Allele Identifier: CA10575647
Gene: IGHM HGNC NCBI

Linked Data

ClinVar Variation Id: 156278
ClinVar RCV Id: RCV000144362
dbSNP Id: rs267606871
MyVariant Identifiers: chr14:g.105854468A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105854468A>C , CM000676.2:g.105854468A>C GRCh38
NC_000014.7:g.105391618A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637539.2:c.1237T>G ENSP00000490253.1:p.Cys413Gly
ENST00000390559.6:c.1237T>G ENSP00000375001.2:p.Cys413Gly
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