Canonical Allele Identifier: CA1672979332
Gene:

Linked Data

dbSNP Id: rs1777189306

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633776C>T , CM000668.2:g.151633776C>T GRCh38
NC_000006.11:g.151954911C>T , CM000668.1:g.151954911C>T GRCh37
NC_000006.10:g.151996604C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3794C>T