Canonical Allele Identifier: CA2378344929
Gene:

Linked Data

dbSNP Id: rs1987465822

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15440842A>G , CM000683.2:g.15440842A>G GRCh38
NC_000021.8:g.16813161A>G , CM000683.1:g.16813161A>G GRCh37
NC_000021.7:g.15735032A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937593.1:n.552+384T>C
XR_001754965.2:n.468+3182T>C
XR_001754970.2:n.468+3182T>C
XR_001754971.2:n.468+3182T>C