Canonical Allele Identifier: CA917706711

Linked Data

dbSNP Id: rs1554256028

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792580_29792598dup , CM000668.2:g.29792580_29792598dup GRCh38
NC_000006.11:g.29760357_29760375dup , CM000668.1:g.29760357_29760375dup GRCh37
NC_000006.10:g.29868336_29868354dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.155_173dup (HCG4)
ENST00000429037.2:n.216_234dup (HLA-V)
ENST00000446817.1:n.326_344dup (HLA-V)
ENST00000457107.5:n.227_245dup (HLA-V)
ENST00000476601.5:n.544_562dup (HLA-V)
NM_001207043.1:c.442_460dup NP_001193972.1:p.Glu154GlyfsTer?
NR_002139.2:n.478_496dup (HCG4)
NR_132323.1:n.544_562dup