Canonical Allele Identifier: CA2607210311
Gene:

Linked Data

dbSNP Id: rs2105755235

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033142A>G , CM000664.2:g.200033142A>G GRCh38
NC_000002.11:g.200897865A>G , CM000664.1:g.200897865A>G GRCh37
NC_000002.10:g.200606110A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22246T>C