Canonical Allele Identifier: CA2729906621
Gene:

Linked Data

dbSNP Id: rs1490773487

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314561C>T , CM000676.2:g.92314561C>T GRCh38
NC_000014.8:g.92780905C>T , CM000676.1:g.92780905C>T GRCh37
NC_000014.7:g.91850658C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-685C>T