Canonical Allele Identifier: CA2607708206
Gene:

Linked Data

dbSNP Id: rs1868335592

Genomic Alleles

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

Transcript Alleles

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