Canonical Allele Identifier: CA1095883570
Gene:

Linked Data

dbSNP Id: rs1777186048

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633568G>T , CM000668.2:g.151633568G>T GRCh38
NC_000006.11:g.151954703G>T , CM000668.1:g.151954703G>T GRCh37
NC_000006.10:g.151996396G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3586G>T