Canonical Allele Identifier: CA378585498
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122506760-G-C
MyVariant Identifiers: chr10:g.124266276G>C (hg19) chr10:g.122506760G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506760G>C , CM000672.2:g.122506760G>C GRCh38
NC_000010.10:g.124266276G>C , CM000672.1:g.124266276G>C GRCh37
NC_000010.9:g.124256266G>C NCBI36
NG_011554.1:g.50236G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.847G>C MANE Select ENSP00000357980.3:p.Gly283Arg
ENST00000648167.1:c.529G>C ENSP00000498033.1:p.Gly177Arg
ENST00000368984.7:c.847G>C ENSP00000357980.3:p.Gly283Arg
ENST00000420892.1:c.70G>C ENSP00000412676.1:p.Gly24Arg
NM_002775.4:c.847G>C NP_002766.1:p.Gly283Arg
NM_002775.5:c.847G>C MANE Select NP_002766.1:p.Gly283Arg
Search 100 bp 5'
Search 100 bp 3'