Canonical Allele Identifier: CA2386425965
Gene:

Linked Data

dbSNP Id: rs2045226000

Genomic Alleles

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

Transcript Alleles

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