Canonical Allele Identifier: CA337528888
Gene:

Linked Data

dbSNP Id: rs9785894

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.21180823A>C , CM000686.2:g.21180823A>C GRCh38
NC_000024.9:g.23342709A>C , CM000686.1:g.23342709A>C GRCh37
NC_000024.8:g.21752097A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001756073.1:n.7279-16317A>C