Canonical Allele Identifier: CA590667409
Gene:

Linked Data

dbSNP Id: rs1364973649

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576795del , CM000671.2:g.129576795del GRCh38
NC_000009.11:g.132339074del , CM000671.1:g.132339074del GRCh37
NC_000009.10:g.131378895del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1197del