Canonical Allele Identifier: CA1181633477
Gene:

Linked Data

dbSNP Id: rs1652358080

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564046T>C , CM000663.2:g.94564046T>C GRCh38
NC_000001.10:g.95029602T>C , CM000663.1:g.95029602T>C GRCh37
NC_000001.9:g.94802190T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+433T>C