Canonical Allele Identifier: CA1677170023
Gene:

Linked Data

dbSNP Id: rs1780353429

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668701del , CM000668.2:g.160668701del GRCh38
NC_000006.11:g.161089733del , CM000668.1:g.161089733del GRCh37
NC_000006.10:g.161009723del NCBI36
NG_016147.1:g.2676del

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2327del