Canonical Allele Identifier: CA1941478032
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1591040887
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508491T>G , CM000672.2:g.122508491T>G GRCh38
NC_000010.10:g.124268007T>G , CM000672.1:g.124268007T>G GRCh37
NC_000010.9:g.124257997T>G NCBI36
NG_011554.1:g.51967T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-165T>G MANE Select ENSP00000357980.3:n.1006-165T>G
ENST00000648167.1:c.688-165T>G ENSP00000498033.1:n.688-165T>G
ENST00000368984.7:c.1006-165T>G ENSP00000357980.3:n.1006-165T>G
ENST00000420892.1:c.229-165T>G ENSP00000412676.1:n.229-165T>G
NM_002775.4:c.1006-165T>G NP_002766.1:n.1006-165T>G
NM_002775.5:c.1006-165T>G MANE Select NP_002766.1:n.1006-165T>G
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