Canonical Allele Identifier: CA1502607166
Gene:

Linked Data

dbSNP Id: rs1732902942

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748298T>C , CM000666.2:g.148748298T>C GRCh38
NC_000004.11:g.149669450T>C , CM000666.1:g.149669450T>C GRCh37
NC_000004.10:g.149888900T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118459T>C