Canonical Allele Identifier: CA1427016153
Gene: AHSG HGNC NCBI

Linked Data

dbSNP Id: rs951149142
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186613084G>A , CM000665.2:g.186613084G>A GRCh38
NC_000003.11:g.186330873G>A , CM000665.1:g.186330873G>A GRCh37
NC_000003.10:g.187813567G>A NCBI36
NG_011436.1:g.5024G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.-58G>A MANE Select ENSP00000393887.2:n.-58G>A
ENST00000273784.5:c.-58G>A ENSP00000273784.5:n.-58G>A
ENST00000411641.6:c.-58G>A ENSP00000393887.2:n.-58G>A
NM_001622.2:c.-58G>A NP_001613.2:n.-58G>A
NM_001354571.1:c.-58G>A NP_001341500.1:n.-58G>A
NM_001354572.1:c.-58G>A NP_001341501.1:n.-58G>A
NM_001354573.1:c.-58G>A NP_001341502.1:n.-58G>A
NM_001622.3:c.-58G>A NP_001613.2:n.-58G>A
NM_001622.4:c.-58G>A MANE Select NP_001613.2:n.-58G>A
NM_001354571.2:c.-58G>A NP_001341500.1:n.-58G>A
NM_001354572.2:c.-58G>A NP_001341501.1:n.-58G>A
NM_001354573.2:c.-58G>A NP_001341502.1:n.-58G>A
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