Canonical Allele Identifier: CA266626965

Gene: IGHG3

Linked Data

• dbSNP Id: rs777835924
• gnomAD v2: 14-106232507-G-A
• gnomAD v3: 14-105766170-G-A
• gnomAD v4: 14-105766170-G-A
• MyVariant Identifiers: chr14:g.106232507G>A (hg19) ; chr14:g.105766170G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105766170G>A , CM000676.2:g.105766170G>A	GRCh38
NC_000014.8:g.106232507G>A , CM000676.1:g.106232507G>A	GRCh37
NC_000014.7:g.105303552G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641136.1:c.1257-173C>T