Canonical Allele Identifier: CA1205766033
Gene:

Linked Data

dbSNP Id: rs1648346245

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649452T>C , CM000663.2:g.168649452T>C GRCh38
NC_000001.10:g.168618690T>C , CM000663.1:g.168618690T>C GRCh37
NC_000001.9:g.166885314T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8177A>G
XR_922259.2:n.332-8177A>G