Canonical Allele Identifier: CA1818161670
Gene:

Linked Data

dbSNP Id: rs1815128038

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012496G>C , CM000670.2:g.127012496G>C GRCh38
NC_000008.10:g.128024741G>C , CM000670.1:g.128024741G>C GRCh37
NC_000008.9:g.128093923G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5878G>C