Canonical Allele Identifier: CA62407684
Gene:

Linked Data

dbSNP Id: rs11678036

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.185160008C>T , CM000664.2:g.185160008C>T GRCh38
NC_000002.11:g.186024735C>T , CM000664.1:g.186024735C>T GRCh37
NC_000002.10:g.185732980C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923664.1:n.151+6843G>A
XR_923665.1:n.151+6843G>A
XR_923666.1:n.151+6843G>A