Canonical Allele Identifier: CA1573442241

Gene:

Linked Data

• ClinVar Variation Id: 1054085
• ClinVar RCV Id: RCV003745319
• dbSNP Id: rs1750555186
• gnomAD v4: 5-112707396-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707396C>T , CM000667.2:g.112707396C>T	GRCh38
NC_000005.9:g.112043093C>T , CM000667.1:g.112043093C>T	GRCh37
NC_000005.8:g.112070992C>T	NCBI36
NG_008481.4:g.19876C>T , LRG_130:g.19876C>T