Canonical Allele Identifier: CA703535466
Gene: IGHG3 HGNC NCBI

Linked Data

dbSNP Id: rs1366243898
gnomAD v3: 14-105766100-T-C
gnomAD v4: 14-105766100-T-C
MyVariant Identifiers: chr14:g.105766100T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105766100T>C , CM000676.2:g.105766100T>C GRCh38
NC_000014.8:g.106232437T>C , CM000676.1:g.106232437T>C GRCh37
NC_000014.7:g.105303482T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641136.1:c.1257-103A>G
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