Canonical Allele Identifier: CA2197752752
Gene:

Linked Data

dbSNP Id: rs1899532616

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782460C>T , CM000677.2:g.95782460C>T GRCh38
NC_000015.9:g.96325689C>T , CM000677.1:g.96325689C>T GRCh37
NC_000015.8:g.94126693C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42729C>T