Canonical Allele Identifier: CA2729910538
Gene:

Linked Data

dbSNP Id: rs1595108874

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314696A>C , CM000676.2:g.92314696A>C GRCh38
NC_000014.8:g.92781040A>C , CM000676.1:g.92781040A>C GRCh37
NC_000014.7:g.91850793A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-550A>C