Canonical Allele Identifier: CA5726028
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs181573207
ExAC: 10:124268151 C / G
gnomAD v2: 10-124268151-C-G
gnomAD v3: 10-122508635-C-G
gnomAD v4: 10-122508635-C-G
MyVariant Identifiers: chr10:g.124268151C>G (hg19) chr10:g.122508635C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508635C>G , CM000672.2:g.122508635C>G GRCh38
NC_000010.10:g.124268151C>G , CM000672.1:g.124268151C>G GRCh37
NC_000010.9:g.124258141C>G NCBI36
NG_011554.1:g.52111C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-21C>G MANE Select ENSP00000357980.3:n.1006-21C>G
ENST00000648167.1:c.688-21C>G ENSP00000498033.1:n.688-21C>G
ENST00000368984.7:c.1006-21C>G ENSP00000357980.3:n.1006-21C>G
ENST00000420892.1:c.229-21C>G ENSP00000412676.1:n.229-21C>G
NM_002775.4:c.1006-21C>G NP_002766.1:n.1006-21C>G
NM_002775.5:c.1006-21C>G MANE Select NP_002766.1:n.1006-21C>G
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