Canonical Allele Identifier: CA266626919
Gene: IGHG3 HGNC NCBI

Linked Data

dbSNP Id: rs368044307
gnomAD v2: 14-106232441-C-T
gnomAD v3: 14-105766104-C-T
gnomAD v4: 14-105766104-C-T
COSMIC: COSN20040037
MyVariant Identifiers: chr14:g.106232441C>T (hg19) chr14:g.105766104C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105766104C>T , CM000676.2:g.105766104C>T GRCh38
NC_000014.8:g.106232441C>T , CM000676.1:g.106232441C>T GRCh37
NC_000014.7:g.105303486C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641136.1:c.1257-107G>A
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