Canonical Allele Identifier: CA1181643449
Gene:

Linked Data

dbSNP Id: rs1570893495

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94587837C>T , CM000663.2:g.94587837C>T GRCh38
NC_000001.10:g.95053393C>T , CM000663.1:g.95053393C>T GRCh37
NC_000001.9:g.94825981C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+24224C>T