Canonical Allele Identifier: CA2193710606
Gene:

Linked Data

dbSNP Id: rs1895002660

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419476G>C , CM000677.2:g.87419476G>C GRCh38
NC_000015.9:g.87962707G>C , CM000677.1:g.87962707G>C GRCh37
NC_000015.8:g.85763711G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-205C>G
XR_932585.1:n.340-205C>G
XR_001751647.1:n.617-205C>G
XR_932585.2:n.627-205C>G