Canonical Allele Identifier: CA2731494730
Gene:

Linked Data

dbSNP Id: rs2141975702

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782352T>C , CM000677.2:g.95782352T>C GRCh38
NC_000015.9:g.96325581T>C , CM000677.1:g.96325581T>C GRCh37
NC_000015.8:g.94126585T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42837T>C