Canonical Allele Identifier: CA14191964
Gene:

Linked Data

dbSNP Id: rs17612678

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.93271900T>C , CM000677.2:g.93271900T>C GRCh38
NC_000015.9:g.93815129T>C , CM000677.1:g.93815129T>C GRCh37
NC_000015.8:g.91616133T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932628.1:n.229+12663T>C
XR_001751669.1:n.229+12663T>C