Canonical Allele Identifier: CA2065107439
Gene:

Linked Data

dbSNP Id: rs1876325191

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398762C>T , CM000674.2:g.115398762C>T GRCh38
NC_000012.11:g.115836567C>T , CM000674.1:g.115836567C>T GRCh37
NC_000012.10:g.114320950C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8333G>A
XR_945389.2:n.701+8333G>A