Canonical Allele Identifier: CA1591798689
Gene:

Linked Data

dbSNP Id: rs1760950842

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354488C>G , CM000667.2:g.152354488C>G GRCh38
NC_000005.9:g.151734049C>G , CM000667.1:g.151734049C>G GRCh37
NC_000005.8:g.151714242C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944433.1:n.196+16625C>G
XR_944433.2:n.197+16625C>G