Canonical Allele Identifier: CA2197256021
Gene:

Linked Data

dbSNP Id: rs1444509595

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775308G>T , CM000677.2:g.94775308G>T GRCh38
NC_000015.9:g.95318537G>T , CM000677.1:g.95318537G>T GRCh37
NC_000015.8:g.93119541G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9291C>A
XR_932644.2:n.369-9291C>A