Canonical Allele Identifier: CA1502607324
Gene:

Linked Data

dbSNP Id: rs1732905448

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748431A>C , CM000666.2:g.148748431A>C GRCh38
NC_000004.11:g.149669583A>C , CM000666.1:g.149669583A>C GRCh37
NC_000004.10:g.149889033A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118326A>C