Canonical Allele Identifier: CA1502607177
Gene:

Linked Data

dbSNP Id: rs1732903840

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748302A>T , CM000666.2:g.148748302A>T GRCh38
NC_000004.11:g.149669454A>T , CM000666.1:g.149669454A>T GRCh37
NC_000004.10:g.149888904A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118455A>T