Canonical Allele Identifier: CA1697889742
Gene:

Linked Data

dbSNP Id: rs1790897436

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897572del , CM000669.2:g.30897572del GRCh38
NC_000007.13:g.30937187del , CM000669.1:g.30937187del GRCh37
NC_000007.12:g.30903712del NCBI36
NG_007475.2:g.49179del

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14421del