Canonical Allele Identifier: CA660865166
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1336699484
gnomAD v3: 10-122461184-G-A
gnomAD v4: 10-122461184-G-A
MyVariant Identifiers: chr10:g.124220700G>A (hg19) chr10:g.122461184G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461184G>A , CM000672.2:g.122461184G>A GRCh38
NC_000010.10:g.124220700G>A , CM000672.1:g.124220700G>A GRCh37
NC_000010.9:g.124210690G>A NCBI36
NG_011554.1:g.4660G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648167.1:c.154+2475G>A ENSP00000498033.1:n.154+2475G>A
XR_946382.1:n.175C>T
XR_946383.1:n.175C>T
XR_946384.1:n.175C>T
XR_946385.1:n.175C>T
XR_946382.2:n.203C>T
XR_946383.2:n.203C>T
XR_946384.2:n.179C>T
XR_946385.2:n.203C>T
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