Canonical Allele Identifier: CA1941477036
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1591039923
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506380T>C , CM000672.2:g.122506380T>C GRCh38
NC_000010.10:g.124265896T>C , CM000672.1:g.124265896T>C GRCh37
NC_000010.9:g.124255886T>C NCBI36
NG_011554.1:g.49856T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-311T>C MANE Select ENSP00000357980.3:n.778-311T>C
ENST00000648167.1:c.460-311T>C ENSP00000498033.1:n.460-311T>C
ENST00000368984.7:c.778-311T>C ENSP00000357980.3:n.778-311T>C
NM_002775.4:c.778-311T>C NP_002766.1:n.778-311T>C
NM_002775.5:c.778-311T>C MANE Select NP_002766.1:n.778-311T>C
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