Canonical Allele Identifier: CA2049072526
Gene:

Linked Data

dbSNP Id: rs1868335858

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069324T>C , CM000674.2:g.80069324T>C GRCh38
NC_000012.11:g.80463104T>C , CM000674.1:g.80463104T>C GRCh37
NC_000012.10:g.78987235T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8142T>C
XR_945141.1:n.1758+8142T>C