Canonical Allele Identifier: CA308127595
Gene:

Linked Data

dbSNP Id: rs990645876
MyVariant Identifiers: chr19:g.38645622C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38645622C>T , CM000681.2:g.38645622C>T GRCh38
NC_000019.9:g.39136262C>T , CM000681.1:g.39136262C>T GRCh37
NC_000019.8:g.43828102C>T NCBI36
NG_007082.2:g.2936C>T