Canonical Allele Identifier: CA2730054358
Gene:

Linked Data

dbSNP Id: rs2139733079

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94944220A>C , CM000676.2:g.94944220A>C GRCh38
NC_000014.8:g.95410557A>C , CM000676.1:g.95410557A>C GRCh37
NC_000014.7:g.94480310A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001750935.1:n.500-291T>G