Canonical Allele Identifier: CA2049072495
Gene:

Linked Data

dbSNP Id: rs1868335592

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069253C>A , CM000674.2:g.80069253C>A GRCh38
NC_000012.11:g.80463033C>A , CM000674.1:g.80463033C>A GRCh37
NC_000012.10:g.78987164C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8071C>A
XR_945141.1:n.1758+8071C>A