Canonical Allele Identifier: CA2701041690
Gene:

Linked Data

dbSNP Id: rs1252589307

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006973A>T , CM000664.2:g.195006973A>T GRCh38
NC_000002.11:g.195871697A>T , CM000664.1:g.195871697A>T GRCh37
NC_000002.10:g.195579942A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52462T>A