Canonical Allele Identifier: CA471669558
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122462078-G-T
MyVariant Identifiers: chr10:g.124221594G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462078G>T , CM000672.2:g.122462078G>T GRCh38
NC_000010.10:g.124221594G>T , CM000672.1:g.124221594G>T GRCh37
NC_000010.9:g.124211584G>T NCBI36
NG_011554.1:g.5554G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.426G>T MANE Select ENSP00000357980.3:p.Leu142=
ENST00000648167.1:c.154+3369G>T ENSP00000498033.1:n.154+3369G>T
ENST00000368984.7:c.426G>T ENSP00000357980.3:p.Leu142=
NM_002775.4:c.426G>T NP_002766.1:p.Leu142=
NM_002775.5:c.426G>T MANE Select NP_002766.1:p.Leu142=
Search 100 bp 5'
Search 100 bp 3'