Canonical Allele Identifier: CA2739826601
Gene: AHSG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186613083G>C , CM000665.2:g.186613083G>C GRCh38
NC_000003.11:g.186330872G>C , CM000665.1:g.186330872G>C GRCh37
NC_000003.10:g.187813566G>C NCBI36
NG_011436.1:g.5023G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.-59G>C MANE Select ENSP00000393887.2:n.-59G>C
ENST00000273784.5:c.-59G>C ENSP00000273784.5:n.-59G>C
ENST00000411641.6:c.-59G>C ENSP00000393887.2:n.-59G>C
NM_001622.2:c.-59G>C NP_001613.2:n.-59G>C
NM_001354571.1:c.-59G>C NP_001341500.1:n.-59G>C
NM_001354572.1:c.-59G>C NP_001341501.1:n.-59G>C
NM_001354573.1:c.-59G>C NP_001341502.1:n.-59G>C
NM_001622.3:c.-59G>C NP_001613.2:n.-59G>C
NM_001622.4:c.-59G>C MANE Select NP_001613.2:n.-59G>C
NM_001354571.2:c.-59G>C NP_001341500.1:n.-59G>C
NM_001354572.2:c.-59G>C NP_001341501.1:n.-59G>C
NM_001354573.2:c.-59G>C NP_001341502.1:n.-59G>C
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