Canonical Allele Identifier: CA1689218059
Gene:

Linked Data

dbSNP Id: rs1783118289

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400553A>G , CM000669.2:g.13400553A>G GRCh38
NC_000007.13:g.13440178A>G , CM000669.1:g.13440178A>G GRCh37
NC_000007.12:g.13406703A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.147+90230A>G