Canonical Allele Identifier: CA535782199
Gene:

Linked Data

dbSNP Id: rs1678951701

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369207_122369213del , CM000664.2:g.122369207_122369213del GRCh38
NC_000002.11:g.123126783_123126789del , CM000664.1:g.123126783_123126789del GRCh37
NC_000002.10:g.122843253_122843259del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23756_556-23750del
XR_001739684.1:n.556-23756_556-23750del