Canonical Allele Identifier: CA1096565205
Gene:

Linked Data

dbSNP Id: rs1361270003

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668694_160668695del , CM000668.2:g.160668694_160668695del GRCh38
NC_000006.11:g.161089726_161089727del , CM000668.1:g.161089726_161089727del GRCh37
NC_000006.10:g.161009716_161009717del NCBI36
NG_016147.1:g.2682_2683del

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2321_115-2320del