Canonical Allele Identifier: CA1905920018
Gene:

Linked Data

dbSNP Id: rs1837179607

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318644T>C , CM000672.2:g.43318644T>C GRCh38
NC_000010.10:g.43814092T>C , CM000672.1:g.43814092T>C GRCh37
NC_000010.9:g.43134098T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+49T>C
XR_945902.2:n.198+49T>C