Canonical Allele Identifier: CA1751305434
Gene:

Linked Data

dbSNP Id: rs1795951905

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148561035A>G , CM000669.2:g.148561035A>G GRCh38
NC_000007.13:g.148258127A>G , CM000669.1:g.148258127A>G GRCh37
NC_000007.12:g.147889060A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7065T>C
XR_928100.1:n.433+7065T>C