Canonical Allele Identifier: CA2728843715
Gene:

Linked Data

dbSNP Id: rs2139095999

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94852990T>C , CM000675.2:g.94852990T>C GRCh38
NC_000013.10:g.95505244T>C , CM000675.1:g.95505244T>C GRCh37
NC_000013.9:g.94303245T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52474T>C