Canonical Allele Identifier: CA1094718405
Gene:

Linked Data

dbSNP Id: rs1774560646

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398917T>C , CM000668.2:g.134398917T>C GRCh38
NC_000006.11:g.134720055T>C , CM000668.1:g.134720055T>C GRCh37
NC_000006.10:g.134761748T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+188T>C