Canonical Allele Identifier: CA1548147791
Gene:

Linked Data

dbSNP Id: rs1748797377

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56899983C>T , CM000667.2:g.56899983C>T GRCh38
NC_000005.9:g.56195810C>T , CM000667.1:g.56195810C>T GRCh37
NC_000005.8:g.56231567C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948346.1:n.83-1687G>A
XR_948347.1:n.76+14G>A
XR_948347.3:n.406+14G>A