Canonical Allele Identifier: CA2381739140
Gene:

Linked Data

dbSNP Id: rs1981477623

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.22259287A>C , CM000683.2:g.22259287A>C GRCh38
NC_000021.8:g.23631607A>C , CM000683.1:g.23631607A>C GRCh37
NC_000021.7:g.22553478A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754978.1:n.221+46474A>C