Canonical Allele Identifier: CA214389666
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs951715520
MyVariant Identifiers: chr10:g.122472105G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472105G>T , CM000672.2:g.122472105G>T GRCh38
NC_000010.10:g.124231621G>T , CM000672.1:g.124231621G>T GRCh37
NC_000010.9:g.124221611G>T NCBI36
NG_011554.1:g.15581G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+9981G>T MANE Select ENSP00000357980.3:n.472+9981G>T
ENST00000648167.1:c.154+13396G>T ENSP00000498033.1:n.154+13396G>T
ENST00000368984.7:c.472+9981G>T ENSP00000357980.3:n.472+9981G>T
NM_002775.4:c.472+9981G>T NP_002766.1:n.472+9981G>T
NM_002775.5:c.472+9981G>T MANE Select NP_002766.1:n.472+9981G>T
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