Canonical Allele Identifier: CA1008923840
Gene:

Linked Data

dbSNP Id: rs1648342072

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649224T>C , CM000663.2:g.168649224T>C GRCh38
NC_000001.10:g.168618462T>C , CM000663.1:g.168618462T>C GRCh37
NC_000001.9:g.166885086T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7949A>G
XR_922259.2:n.332-7949A>G