Canonical Allele Identifier: CA2386425927
Gene:

Linked Data

dbSNP Id: rs2045225629

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890326G>C , CM000683.2:g.32890326G>C GRCh38
NC_000021.8:g.34262634G>C , CM000683.1:g.34262634G>C GRCh37
NC_000021.7:g.33184504G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937669.1:n.460-3252G>C
XR_937669.2:n.1038-3252G>C