Canonical Allele Identifier: CA1205765973
Gene:

Linked Data

dbSNP Id: rs1648343667

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649330A>C , CM000663.2:g.168649330A>C GRCh38
NC_000001.10:g.168618568A>C , CM000663.1:g.168618568A>C GRCh37
NC_000001.9:g.166885192A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8055T>G
XR_922259.2:n.332-8055T>G