Canonical Allele Identifier: CA266626982

Gene: IGHG3

Linked Data

• dbSNP Id: rs757784683
• gnomAD v2: 14-106232559-G-C
• gnomAD v3: 14-105766222-G-C
• gnomAD v4: 14-105766222-G-C
• MyVariant Identifiers: chr14:g.106232559G>C (hg19) ; chr14:g.105766222G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105766222G>C , CM000676.2:g.105766222G>C	GRCh38
NC_000014.8:g.106232559G>C , CM000676.1:g.106232559G>C	GRCh37
NC_000014.7:g.105303604G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641136.1:c.1257-225C>G