Canonical Allele Identifier: CA2141801104
Gene:

Linked Data

dbSNP Id: rs1883742882

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501597T>C , CM000676.2:g.62501597T>C GRCh38
NC_000014.8:g.62968315T>C , CM000676.1:g.62968315T>C GRCh37
NC_000014.7:g.62038068T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2444T>C
XR_943932.2:n.103-2444T>C