Canonical Allele Identifier: CA977150973
Gene:

Linked Data

dbSNP Id: rs1961465273

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108502A>G , CM000678.2:g.49108502A>G GRCh38
NC_000016.9:g.49142413A>G , CM000678.1:g.49142413A>G GRCh37
NC_000016.8:g.47699914A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1442T>C
XR_001752138.2:n.591+5474T>C
XR_933517.2:n.810+1442T>C