Canonical Allele Identifier: CA2136398873
Gene:

Linked Data

dbSNP Id: rs1595986777

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856911A>C , CM000676.2:g.50856911A>C GRCh38
NC_000014.8:g.51323629A>C , CM000676.1:g.51323629A>C GRCh37
NC_000014.7:g.50393379A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1187T>G
XR_943848.2:n.643+1187T>G