Canonical Allele Identifier: CA1941478264
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097504414
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122509054T>C , CM000672.2:g.122509054T>C GRCh38
NC_000010.10:g.124268570T>C , CM000672.1:g.124268570T>C GRCh37
NC_000010.9:g.124258560T>C NCBI36
NG_011554.1:g.52530T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1120+284T>C MANE Select ENSP00000357980.3:n.1120+284T>C
ENST00000648167.1:c.802+284T>C ENSP00000498033.1:n.802+284T>C
ENST00000368984.7:c.1120+284T>C ENSP00000357980.3:n.1120+284T>C
ENST00000420892.1:c.343+284T>C ENSP00000412676.1:n.343+284T>C
NM_002775.4:c.1120+284T>C NP_002766.1:n.1120+284T>C
NM_002775.5:c.1120+284T>C MANE Select NP_002766.1:n.1120+284T>C
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