Canonical Allele Identifier: CA2700885285
Gene:

Linked Data

dbSNP Id: rs2105300771

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260461C>T , CM000664.2:g.168260461C>T GRCh38
NC_000002.11:g.169116971C>T , CM000664.1:g.169116971C>T GRCh37
NC_000002.10:g.168825217C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4635C>T
XR_001739764.1:n.318-4635C>T
XR_001739765.1:n.436-4635C>T