Canonical Allele Identifier: CA1320446070
Gene:

Linked Data

dbSNP Id: rs2077888405

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033019C>G , CM000664.2:g.200033019C>G GRCh38
NC_000002.11:g.200897742C>G , CM000664.1:g.200897742C>G GRCh37
NC_000002.10:g.200605987C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22123G>C