Canonical Allele Identifier: CA214412535
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs947987594
gnomAD v3: 10-122508634-C-T
gnomAD v4: 10-122508634-C-T
MyVariant Identifiers: chr10:g.124268150C>T (hg19) chr10:g.122508634C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508634C>T , CM000672.2:g.122508634C>T GRCh38
NC_000010.10:g.124268150C>T , CM000672.1:g.124268150C>T GRCh37
NC_000010.9:g.124258140C>T NCBI36
NG_011554.1:g.52110C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-22C>T MANE Select ENSP00000357980.3:n.1006-22C>T
ENST00000648167.1:c.688-22C>T ENSP00000498033.1:n.688-22C>T
ENST00000368984.7:c.1006-22C>T ENSP00000357980.3:n.1006-22C>T
ENST00000420892.1:c.229-22C>T ENSP00000412676.1:n.229-22C>T
NM_002775.4:c.1006-22C>T NP_002766.1:n.1006-22C>T
NM_002775.5:c.1006-22C>T MANE Select NP_002766.1:n.1006-22C>T
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