Canonical Allele Identifier: CA2729921744
Gene:

Linked Data

dbSNP Id: rs1884565233

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307317G>T , CM000676.2:g.92307317G>T GRCh38
NC_000014.8:g.92773661G>T , CM000676.1:g.92773661G>T GRCh37
NC_000014.7:g.91843414G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2773G>T