Canonical Allele Identifier: CA1206219189
Gene: FIRRM HGNC NCBI
SELE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169737031_169737032delinsGA , CM000663.2:g.169737031_169737032delinsGA GRCh38
NC_000001.10:g.169706172_169706173delinsGA , CM000663.1:g.169706172_169706173delinsGA GRCh37
NC_000001.9:g.167972796_167972797delinsGA NCBI36
NG_012124.1:g.2048_2049delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.852-46780_852-46779delinsGA (FIRRM)
ENST00000609271.1:c.-201-2909_-201-2908delinsTC (SELE) ENSP00000476784.1:n.-201-2909_-201-2908delinsTC
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