Canonical Allele Identifier: CA1674885539
Gene:

Linked Data

dbSNP Id: rs1778854013

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812306del , CM000668.2:g.155812306del GRCh38
NC_000006.11:g.156133440del , CM000668.1:g.156133440del GRCh37
NC_000006.10:g.156175132del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18887del
XR_943146.1:n.645-267del
XR_001744423.1:n.699-267del
XR_001744424.1:n.79+18887del