Canonical Allele Identifier: CA207989728
Gene:

Linked Data

dbSNP Id: rs566305134

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812872A>G , CM000672.2:g.57812872A>G GRCh38
NC_000010.10:g.59572632A>G , CM000672.1:g.59572632A>G GRCh37
NC_000010.9:g.59242638A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34420T>C
XR_001747454.1:n.85+34420T>C