Canonical Allele Identifier: CA2193710557
Gene:

Linked Data

dbSNP Id: rs1596084738

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419458G>C , CM000677.2:g.87419458G>C GRCh38
NC_000015.9:g.87962689G>C , CM000677.1:g.87962689G>C GRCh37
NC_000015.8:g.85763693G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-187C>G
XR_932585.1:n.340-187C>G
XR_001751647.1:n.617-187C>G
XR_932585.2:n.627-187C>G