Canonical Allele Identifier: CA926324540
Gene:

Linked Data

dbSNP Id: rs1835465240

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075820T>C , CM000672.2:g.29075820T>C GRCh38
NC_000010.10:g.29364749T>C , CM000672.1:g.29364749T>C GRCh37
NC_000010.9:g.29404755T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3672T>C