Canonical Allele Identifier: CA916336570
Gene: FIRRM HGNC NCBI
SELE HGNC NCBI

Linked Data

dbSNP Id: rs1553243348
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169736941_169736942delinsGG , CM000663.2:g.169736941_169736942delinsGG GRCh38
NC_000001.10:g.169706082_169706083delinsGG , CM000663.1:g.169706082_169706083delinsGG GRCh37
NC_000001.9:g.167972706_167972707delinsGG NCBI36
NG_012124.1:g.2138_2139delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.852-46870_852-46869delinsGG (FIRRM)
ENST00000609271.1:c.-201-2819_-201-2818delinsCC (SELE) ENSP00000476784.1:n.-201-2819_-201-2818delinsCC
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