Canonical Allele Identifier: CA2024154206
Gene:

Linked Data

dbSNP Id: rs1591873945

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045145C>T , CM000674.2:g.28045145C>T GRCh38
NC_000012.11:g.28198078C>T , CM000674.1:g.28198078C>T GRCh37
NC_000012.10:g.28089345C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931460.1:n.154-6187G>A