Canonical Allele Identifier: CA1818149986
Gene:

Linked Data

dbSNP Id: rs1814940176

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999820A>C , CM000670.2:g.126999820A>C GRCh38
NC_000008.10:g.128012065A>C , CM000670.1:g.128012065A>C GRCh37
NC_000008.9:g.128081247A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6735A>C