ClinGen Allele Registry
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Canonical Allele Identifier:
CA616277133
Gene: IGHG3
HGNC
NCBI
Linked Data
dbSNP Id:
rs1352727128
gnomAD v2:
14-106232530-T-C
gnomAD v3:
14-105766193-T-C
gnomAD v4:
14-105766193-T-C
MyVariant Identifiers:
chr14:g.106232530T>C (hg19)
chr14:g.105766193T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.105766193T>C , CM000676.2:g.105766193T>C
GRCh38
NC_000014.8:g.106232530T>C , CM000676.1:g.106232530T>C
GRCh37
NC_000014.7:g.105303575T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000641136.1:c.1257-196A>G
Search 100 bp 5'
Search 100 bp 3'