Canonical Allele Identifier: CA1206219165
Gene: FIRRM HGNC NCBI
SELE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169736976_169736977delinsAG , CM000663.2:g.169736976_169736977delinsAG GRCh38
NC_000001.10:g.169706117_169706118delinsAG , CM000663.1:g.169706117_169706118delinsAG GRCh37
NC_000001.9:g.167972741_167972742delinsAG NCBI36
NG_012124.1:g.2103_2104delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.852-46835_852-46834delinsAG (FIRRM)
ENST00000609271.1:c.-201-2854_-201-2853delinsCT (SELE) ENSP00000476784.1:n.-201-2854_-201-2853delinsCT
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