Canonical Allele Identifier: CA1818161768
Gene:

Linked Data

dbSNP Id: rs1815129947

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012596T>C , CM000670.2:g.127012596T>C GRCh38
NC_000008.10:g.128024841T>C , CM000670.1:g.128024841T>C GRCh37
NC_000008.9:g.128094023T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1364+5978T>C