Canonical Allele Identifier: CA266543329
Gene: IGHM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105855988G>C , CM000676.2:g.105855988G>C GRCh38
NC_000014.7:g.105393138G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000390559.6:c.231C>G ENSP00000375001.2:p.Asp77Glu
ENST00000637539.2:c.231C>G ENSP00000490253.1:p.Asp77Glu
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