Canonical Allele Identifier: CA2606860786

Gene: AHSG

Linked Data

• dbSNP Id: rs2108502449
• gnomAD v3: 3-186618372-CA-C
• gnomAD v4: 3-186618372-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618373del , CM000665.2:g.186618373del	GRCh38
NC_000003.11:g.186336162del , CM000665.1:g.186336162del	GRCh37
NC_000003.10:g.187818856del	NCBI36
NG_011436.1:g.10313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-163del MANE Select	ENSP00000393887.2:n.574-163del
ENST00000273784.5:c.577-163del	ENSP00000273784.5:n.577-163del
ENST00000411641.6:c.574-163del	ENSP00000393887.2:n.574-163del
NM_001622.2:c.574-163del	NP_001613.2:n.574-163del
NM_001354571.1:c.577-163del	NP_001341500.1:n.577-163del
NM_001354572.1:c.571-163del	NP_001341501.1:n.571-163del
NM_001354573.1:c.574-163del	NP_001341502.1:n.574-163del
NM_001622.3:c.574-163del	NP_001613.2:n.574-163del
NM_001622.4:c.574-163del MANE Select	NP_001613.2:n.574-163del
NM_001354571.2:c.577-163del	NP_001341500.1:n.577-163del
NM_001354572.2:c.571-163del	NP_001341501.1:n.571-163del
NM_001354573.2:c.574-163del	NP_001341502.1:n.574-163del