Canonical Allele Identifier: CA721212601
Gene:

Linked Data

dbSNP Id: rs1287047545

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108719T>C , CM000678.2:g.49108719T>C GRCh38
NC_000016.9:g.49142630T>C , CM000678.1:g.49142630T>C GRCh37
NC_000016.8:g.47700131T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1225A>G
XR_001752138.2:n.591+5257A>G
XR_933517.2:n.810+1225A>G