Canonical Allele Identifier: CA308572822
Gene:

Linked Data

dbSNP Id: rs1428922
MyVariant Identifiers: chr19:g.41875710A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41875710A>G , CM000681.2:g.41875710A>G GRCh38