Canonical Allele Identifier: CA1438624479
Gene:

Linked Data

dbSNP Id: rs1713317828

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11501897C>G , CM000666.2:g.11501897C>G GRCh38
NC_000004.11:g.11503521C>G , CM000666.1:g.11503521C>G GRCh37
NC_000004.10:g.11112619C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741361.1:n.950+19051C>G