Canonical Allele Identifier: CA916645607
Gene:

Linked Data

dbSNP Id: rs1573464709

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431640dup , CM000664.2:g.127431640dup GRCh38
NC_000002.11:g.128189216dup , CM000664.1:g.128189216dup GRCh37
NC_000002.10:g.127905686dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+30dup
XR_001739705.1:n.3607-3373dup
XR_923313.2:n.4042+30dup