Canonical Allele Identifier: CA1040809100
Gene:

Linked Data

dbSNP Id: rs1688120489

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007078A>C , CM000664.2:g.195007078A>C GRCh38
NC_000002.11:g.195871802A>C , CM000664.1:g.195871802A>C GRCh37
NC_000002.10:g.195580047A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52357T>G