ClinGen Allele Registry
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Canonical Allele Identifier:
CA703535489
Gene: IGHG3
HGNC
NCBI
Linked Data
dbSNP Id:
rs1199289066
gnomAD v3:
14-105766114-T-G
gnomAD v4:
14-105766114-T-G
MyVariant Identifiers:
chr14:g.105766114T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.105766114T>G , CM000676.2:g.105766114T>G
GRCh38
NC_000014.8:g.106232451T>G , CM000676.1:g.106232451T>G
GRCh37
NC_000014.7:g.105303496T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000641136.1:c.1257-117A>C
Search 100 bp 5'
Search 100 bp 3'