Canonical Allele Identifier: CA2381739129
Gene:

Linked Data

dbSNP Id: rs1981476475

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.22259269A>T , CM000683.2:g.22259269A>T GRCh38
NC_000021.8:g.23631589A>T , CM000683.1:g.23631589A>T GRCh37
NC_000021.7:g.22553460A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754978.1:n.221+46456A>T