Canonical Allele Identifier: CA1841175578
Gene:

Linked Data

dbSNP Id: rs1586967791

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551425G>C , CM000671.2:g.25551425G>C GRCh38
NC_000009.11:g.25551423G>C , CM000671.1:g.25551423G>C GRCh37
NC_000009.10:g.25541423G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-853C>G
XR_929525.2:n.674-853C>G