Canonical Allele Identifier: CA214411489
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs375931183
gnomAD v2: 10-124266423-G-T
gnomAD v3: 10-122506907-G-T
gnomAD v4: 10-122506907-G-T
MyVariant Identifiers: chr10:g.124266423G>T (hg19) chr10:g.122506907G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506907G>T , CM000672.2:g.122506907G>T GRCh38
NC_000010.10:g.124266423G>T , CM000672.1:g.124266423G>T GRCh37
NC_000010.9:g.124256413G>T NCBI36
NG_011554.1:g.50383G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+22G>T MANE Select ENSP00000357980.3:n.972+22G>T
ENST00000648167.1:c.654+22G>T ENSP00000498033.1:n.654+22G>T
ENST00000368984.7:c.972+22G>T ENSP00000357980.3:n.972+22G>T
ENST00000420892.1:c.195+22G>T ENSP00000412676.1:n.195+22G>T
NM_002775.4:c.972+22G>T NP_002766.1:n.972+22G>T
NM_002775.5:c.972+22G>T MANE Select NP_002766.1:n.972+22G>T
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