Canonical Allele Identifier: CA2136398933
Gene:

Linked Data

dbSNP Id: rs1240105563

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857030G>T , CM000676.2:g.50857030G>T GRCh38
NC_000014.8:g.51323748G>T , CM000676.1:g.51323748G>T GRCh37
NC_000014.7:g.50393498G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1068C>A
XR_943848.2:n.643+1068C>A