Canonical Allele Identifier: CA1021899205
Gene:

Linked Data

dbSNP Id: rs2045226000

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890415G>A , CM000683.2:g.32890415G>A GRCh38
NC_000021.8:g.34262723G>A , CM000683.1:g.34262723G>A GRCh37
NC_000021.7:g.33184593G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937669.1:n.460-3163G>A
XR_937669.2:n.1038-3163G>A