Canonical Allele Identifier: CA304896069
Gene:

Linked Data

dbSNP Id: rs1050610044
gnomAD v4: 19-7669032-C-T
MyVariant Identifiers: chr19:g.7669032C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669032C>T , CM000681.2:g.7669032C>T GRCh38
NC_000019.9:g.7733918C>T , CM000681.1:g.7733918C>T GRCh37
NC_000019.8:g.7639918C>T NCBI36
NG_023447.1:g.4947C>T