Canonical Allele Identifier: CA136859136
Gene:

Linked Data

dbSNP Id: rs1554240078

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440119del , CM000668.2:g.31440119del GRCh38
NC_000006.11:g.31407896del , CM000668.1:g.31407896del GRCh37
NC_000006.10:g.31515875del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-67del