Canonical Allele Identifier: CA2135545203
Gene:

Linked Data

dbSNP Id: rs1880002440

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49067759G>A , CM000676.2:g.49067759G>A GRCh38
NC_000014.8:g.49534477G>A , CM000676.1:g.49534477G>A GRCh37
NC_000014.7:g.48604227G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943837.1:n.222+2033C>T
XR_943837.2:n.345+2033C>T