Canonical Allele Identifier: CA276104129
Gene:

Linked Data

dbSNP Id: rs183829878

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782458C>T , CM000677.2:g.95782458C>T GRCh38
NC_000015.9:g.96325687C>T , CM000677.1:g.96325687C>T GRCh37
NC_000015.8:g.94126691C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42731C>T