Canonical Allele Identifier: CA2386425949
Gene:

Linked Data

dbSNP Id: rs2045225813

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890380T>C , CM000683.2:g.32890380T>C GRCh38
NC_000021.8:g.34262688T>C , CM000683.1:g.34262688T>C GRCh37
NC_000021.7:g.33184558T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937669.1:n.460-3198T>C
XR_937669.2:n.1038-3198T>C