Canonical Allele Identifier: CA1557963462
Gene:

Linked Data

dbSNP Id: rs1753648014

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79550019C>T , CM000667.2:g.79550019C>T GRCh38
NC_000005.9:g.78845842C>T , CM000667.1:g.78845842C>T GRCh37
NC_000005.8:g.78881598C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948497.1:n.72+2375C>T
XR_948498.1:n.159+2182C>T
XR_948499.1:n.67+1717C>T
XR_948497.2:n.72+2375C>T
XR_948498.2:n.159+2182C>T
XR_948499.2:n.225+1717C>T