Canonical Allele Identifier: CA703535639
Gene: IGHG3 HGNC NCBI

Linked Data

dbSNP Id: rs1270814198
MyVariant Identifiers: chr14:g.105766223G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105766223G>T , CM000676.2:g.105766223G>T GRCh38
NC_000014.8:g.106232560G>T , CM000676.1:g.106232560G>T GRCh37
NC_000014.7:g.105303605G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641136.1:c.1257-226C>A