Canonical Allele Identifier: CA882371966
Gene:

Linked Data

dbSNP Id: rs1462480441
MyVariant Identifiers: chr19:g.41648274A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648274A>G , CM000681.2:g.41648274A>G GRCh38
NC_000019.9:g.42152195A>G , CM000681.1:g.42152195A>G GRCh37
NC_000019.8:g.46844035A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3228T>C