Canonical Allele Identifier: CA214414529
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs984283619
MyVariant Identifiers: chr10:g.122460904A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122460904A>G , CM000672.2:g.122460904A>G GRCh38
NC_000010.10:g.124220420A>G , CM000672.1:g.124220420A>G GRCh37
NC_000010.9:g.124210410A>G NCBI36
NG_011554.1:g.4380A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2195A>G ENSP00000498033.1:n.154+2195A>G
XR_946382.1:n.410+45T>C
XR_946383.1:n.410+45T>C
XR_946384.1:n.410+45T>C
XR_946385.1:n.410+45T>C
XR_946382.2:n.438+45T>C
XR_946383.2:n.438+45T>C
XR_946384.2:n.414+45T>C
XR_946385.2:n.438+45T>C