Canonical Allele Identifier: CA2129379076
Gene:

Linked Data

dbSNP Id: rs918421976

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384930T>C , CM000676.2:g.36384930T>C GRCh38
NC_000014.8:g.36854135T>C , CM000676.1:g.36854135T>C GRCh37
NC_000014.7:g.35923886T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12229T>C XP_011535730.1:n.319-12229T>C
XR_943756.1:n.358+23834T>C