Canonical Allele Identifier: CA1591798737
Gene:

Linked Data

dbSNP Id: rs1670224899

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354609T>C , CM000667.2:g.152354609T>C GRCh38
NC_000005.9:g.151734170T>C , CM000667.1:g.151734170T>C GRCh37
NC_000005.8:g.151714363T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16746T>C
XR_944433.2:n.197+16746T>C