Canonical Allele Identifier: CA1912720967
Gene:

Linked Data

dbSNP Id: rs1839462653

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57813015_57813016del , CM000672.2:g.57813015_57813016del GRCh38
NC_000010.10:g.59572775_59572776del , CM000672.1:g.59572775_59572776del GRCh37
NC_000010.9:g.59242781_59242782del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34279_68+34280del
XR_001747454.1:n.85+34279_85+34280del