Canonical Allele Identifier: CA266741838
Gene: IGHV3-49 HGNC NCBI
MyVariant.info:
GRCh38 chr14:g.106600343G>A
gnomAD v3:
14:106600343 G / A
gnomAD v4:
chr14-106600343-G-A
Joint Max Group AF 0.45846165 (AMR)
Genomes Max Group AF 0.45846165 (AMR)
dbSNP:
2003168
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.106600343G>A , CM000676.2:g.106600343G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000613477.1:c.14-43095C>T ENSP00000478467.1:n.14-43095C>T
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