Canonical Allele Identifier: CA2141801122
Gene:

Linked Data

dbSNP Id: rs1883743471

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501613A>G , CM000676.2:g.62501613A>G GRCh38
NC_000014.8:g.62968331A>G , CM000676.1:g.62968331A>G GRCh37
NC_000014.7:g.62038084A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2428A>G
XR_943932.2:n.103-2428A>G