Canonical Allele Identifier: CA2345843990
Gene:

Linked Data

dbSNP Id: rs1983026685

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875477C>G , CM000682.2:g.1875477C>G GRCh38
NC_000020.10:g.1856123C>G , CM000682.1:g.1856123C>G GRCh37
NC_000020.9:g.1804123C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754467.1:n.433-7384G>C