Canonical Allele Identifier: CA1502607306
Gene:

Linked Data

dbSNP Id: rs1579426457

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748417C>A , CM000666.2:g.148748417C>A GRCh38
NC_000004.11:g.149669569C>A , CM000666.1:g.149669569C>A GRCh37
NC_000004.10:g.149889019C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118340C>A