Canonical Allele Identifier: CA1095883665
Gene:

Linked Data

dbSNP Id: rs1777189237

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633765G>T , CM000668.2:g.151633765G>T GRCh38
NC_000006.11:g.151954900G>T , CM000668.1:g.151954900G>T GRCh37
NC_000006.10:g.151996593G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3783G>T