Canonical Allele Identifier: CA847111683
Gene:

Linked Data

dbSNP Id: rs1432608203

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999650T>C , CM000670.2:g.126999650T>C GRCh38
NC_000008.10:g.128011895T>C , CM000670.1:g.128011895T>C GRCh37
NC_000008.9:g.128081077T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6905T>C