Canonical Allele Identifier: CA703535471
Gene: IGHG3 HGNC NCBI

Linked Data

dbSNP Id: rs1305089322
MyVariant Identifiers: chr14:g.105766101A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105766101A>G , CM000676.2:g.105766101A>G GRCh38
NC_000014.8:g.106232438A>G , CM000676.1:g.106232438A>G GRCh37
NC_000014.7:g.105303483A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641136.1:c.1257-104T>C