Canonical Allele Identifier: CA660864988
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs934047471
gnomAD v3: 10-122461017-T-C
gnomAD v4: 10-122461017-T-C
MyVariant Identifiers: chr10:g.124220533T>C (hg19) chr10:g.122461017T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461017T>C , CM000672.2:g.122461017T>C GRCh38
NC_000010.10:g.124220533T>C , CM000672.1:g.124220533T>C GRCh37
NC_000010.9:g.124210523T>C NCBI36
NG_011554.1:g.4493T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648167.1:c.154+2308T>C ENSP00000498033.1:n.154+2308T>C
XR_946382.1:n.342A>G
XR_946383.1:n.342A>G
XR_946384.1:n.342A>G
XR_946385.1:n.342A>G
XR_946382.2:n.370A>G
XR_946383.2:n.370A>G
XR_946384.2:n.346A>G
XR_946385.2:n.370A>G
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