Canonical Allele Identifier: CA2221132903
Gene:

Linked Data

dbSNP Id: rs1596728244

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108866T>C , CM000678.2:g.49108866T>C GRCh38
NC_000016.9:g.49142777T>C , CM000678.1:g.49142777T>C GRCh37
NC_000016.8:g.47700278T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1078A>G
XR_001752138.2:n.591+5110A>G
XR_933517.2:n.810+1078A>G