Canonical Allele Identifier: CA2136398848
Gene:

Linked Data

dbSNP Id: rs2045893507

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856846C>G , CM000676.2:g.50856846C>G GRCh38
NC_000014.8:g.51323564C>G , CM000676.1:g.51323564C>G GRCh37
NC_000014.7:g.50393314C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1252G>C
XR_943848.2:n.643+1252G>C