Canonical Allele Identifier: CA471666574
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266218T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506702T>G , CM000672.2:g.122506702T>G GRCh38
NC_000010.10:g.124266218T>G , CM000672.1:g.124266218T>G GRCh37
NC_000010.9:g.124256208T>G NCBI36
NG_011554.1:g.50178T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.789T>G MANE Select ENSP00000357980.3:p.Pro263=
ENST00000648167.1:c.471T>G ENSP00000498033.1:p.Pro157=
ENST00000368984.7:c.789T>G ENSP00000357980.3:p.Pro263=
ENST00000420892.1:c.12T>G ENSP00000412676.1:p.Pro4=
NM_002775.4:c.789T>G NP_002766.1:p.Pro263=
NM_002775.5:c.789T>G MANE Select NP_002766.1:p.Pro263=
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Search 100 bp 3'