Canonical Allele Identifier: CA1439212881
Gene:

Linked Data

dbSNP Id: rs1711589954

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578251_12578254del , CM000666.2:g.12578251_12578254del GRCh38
NC_000004.11:g.12579875_12579878del , CM000666.1:g.12579875_12579878del GRCh37
NC_000004.10:g.12188973_12188976del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31092_106+31095del
XR_001741374.1:n.254+44405_254+44408del
XR_925406.3:n.140+31092_140+31095del