Canonical Allele Identifier: CA917088041
Gene: AHSG HGNC NCBI

Linked Data

dbSNP Id: rs1560250994
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186618301_186618302dup , CM000665.2:g.186618301_186618302dup GRCh38
NC_000003.11:g.186336090_186336091dup , CM000665.1:g.186336090_186336091dup GRCh37
NC_000003.10:g.187818784_187818785dup NCBI36
NG_011436.1:g.10241_10242dup

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.574-235_574-234dup MANE Select ENSP00000393887.2:n.574-235_574-234dup
ENST00000273784.5:c.577-235_577-234dup ENSP00000273784.5:n.577-235_577-234dup
ENST00000411641.6:c.574-235_574-234dup ENSP00000393887.2:n.574-235_574-234dup
NM_001622.2:c.574-235_574-234dup NP_001613.2:n.574-235_574-234dup
NM_001354571.1:c.577-235_577-234dup NP_001341500.1:n.577-235_577-234dup
NM_001354572.1:c.571-235_571-234dup NP_001341501.1:n.571-235_571-234dup
NM_001354573.1:c.574-235_574-234dup NP_001341502.1:n.574-235_574-234dup
NM_001622.3:c.574-235_574-234dup NP_001613.2:n.574-235_574-234dup
NM_001622.4:c.574-235_574-234dup MANE Select NP_001613.2:n.574-235_574-234dup
NM_001354571.2:c.577-235_577-234dup NP_001341500.1:n.577-235_577-234dup
NM_001354572.2:c.571-235_571-234dup NP_001341501.1:n.571-235_571-234dup
NM_001354573.2:c.574-235_574-234dup NP_001341502.1:n.574-235_574-234dup
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