Canonical Allele Identifier: CA978092293
Gene:

Linked Data

dbSNP Id: rs2962462

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.62764948G>C , CM000678.2:g.62764948G>C GRCh38
NC_000016.9:g.62798852G>C , CM000678.1:g.62798852G>C GRCh37
NC_000016.8:g.61356353G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_429756.2:n.133-4044G>C
XR_933661.1:n.133-4044G>C
XR_933663.1:n.260-4044G>C
XR_933661.2:n.133-4044G>C
XR_933663.2:n.260-4044G>C