Canonical Allele Identifier: CA1591798705
Gene:

Linked Data

dbSNP Id: rs1760951211

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354530G>T , CM000667.2:g.152354530G>T GRCh38
NC_000005.9:g.151734091G>T , CM000667.1:g.151734091G>T GRCh37
NC_000005.8:g.151714284G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16667G>T
XR_944433.2:n.197+16667G>T