Canonical Allele Identifier: CA882371969
Gene:

Linked Data

dbSNP Id: rs1240942728
MyVariant Identifiers: chr19:g.41648282G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648282G>A , CM000681.2:g.41648282G>A GRCh38
NC_000019.9:g.42152203G>A , CM000681.1:g.42152203G>A GRCh37
NC_000019.8:g.46844043G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3220C>T