Canonical Allele Identifier: CA2049072528
Gene:

Linked Data

dbSNP Id: rs1868335866

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069325C>T , CM000674.2:g.80069325C>T GRCh38
NC_000012.11:g.80463105C>T , CM000674.1:g.80463105C>T GRCh37
NC_000012.10:g.78987236C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8143C>T
XR_945141.1:n.1758+8143C>T