Canonical Allele Identifier: CA266626873

Gene: IGHG3

Linked Data

• dbSNP Id: rs994160706
• gnomAD v2: 14-106232391-T-C
• gnomAD v3: 14-105766054-T-C
• gnomAD v4: 14-105766054-T-C
• MyVariant Identifiers: chr14:g.106232391T>C (hg19) ; chr14:g.105766054T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105766054T>C , CM000676.2:g.105766054T>C	GRCh38
NC_000014.8:g.106232391T>C , CM000676.1:g.106232391T>C	GRCh37
NC_000014.7:g.105303436T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641136.1:c.1257-57A>G