Canonical Allele Identifier: CA1095883557
Gene:

Linked Data

dbSNP Id: rs1777185905

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633525T>A , CM000668.2:g.151633525T>A GRCh38
NC_000006.11:g.151954660T>A , CM000668.1:g.151954660T>A GRCh37
NC_000006.10:g.151996353T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3543T>A