Canonical Allele Identifier: CA1305906752
Gene:

Linked Data

dbSNP Id: rs1691191466

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260469C>T , CM000664.2:g.168260469C>T GRCh38
NC_000002.11:g.169116979C>T , CM000664.1:g.169116979C>T GRCh37
NC_000002.10:g.168825225C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4627C>T
XR_001739764.1:n.318-4627C>T
XR_001739765.1:n.436-4627C>T