Canonical Allele Identifier: CA1095883565
Gene:

Linked Data

dbSNP Id: rs1777186002

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633558C>A , CM000668.2:g.151633558C>A GRCh38
NC_000006.11:g.151954693C>A , CM000668.1:g.151954693C>A GRCh37
NC_000006.10:g.151996386C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3576C>A