Canonical Allele Identifier: CA1619157186
Gene:

Linked Data

dbSNP Id: rs1761793889

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440074C>T , CM000668.2:g.31440074C>T GRCh38
NC_000006.11:g.31407851C>T , CM000668.1:g.31407851C>T GRCh37
NC_000006.10:g.31515830C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-22G>A