Canonical Allele Identifier: CA378606391
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124221591G>C (hg19) chr10:g.122462075G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462075G>C , CM000672.2:g.122462075G>C GRCh38
NC_000010.10:g.124221591G>C , CM000672.1:g.124221591G>C GRCh37
NC_000010.9:g.124211581G>C NCBI36
NG_011554.1:g.5551G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.423G>C MANE Select ENSP00000357980.3:p.Arg141Ser
ENST00000648167.1:c.154+3366G>C ENSP00000498033.1:n.154+3366G>C
ENST00000368984.7:c.423G>C ENSP00000357980.3:p.Arg141Ser
NM_002775.4:c.423G>C NP_002766.1:p.Arg141Ser
NM_002775.5:c.423G>C MANE Select NP_002766.1:p.Arg141Ser
Search 100 bp 5'
Search 100 bp 3'