Allele Registry

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Canonical Allele Identifier: CA10575525

Gene: IGHM HGNC NCBI

Linked Data

ClinVar Variation Id: 14813

ClinVar RCV Id: RCV000015936

dbSNP Id: rs281865422

MyVariant Identifiers: chr14:g.105855107C>T (hg38)

PubMed: PMID:12370281

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105855107C>T , CM000676.2:g.105855107C>T	GRCh38
NC_000014.7:g.105392257C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637539.2:c.777G>A	ENSP00000490253.1:p.Trp259Ter
ENST00000390559.6:c.777G>A	ENSP00000375001.2:p.Trp259Ter

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