Canonical Allele Identifier: CA214411679
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs913532898
MyVariant Identifiers: chr10:g.122507202G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507202G>T , CM000672.2:g.122507202G>T GRCh38
NC_000010.10:g.124266718G>T , CM000672.1:g.124266718G>T GRCh37
NC_000010.9:g.124256708G>T NCBI36
NG_011554.1:g.50678G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-168G>T MANE Select ENSP00000357980.3:n.973-168G>T
ENST00000648167.1:c.655-168G>T ENSP00000498033.1:n.655-168G>T
ENST00000368984.7:c.973-168G>T ENSP00000357980.3:n.973-168G>T
ENST00000420892.1:c.196-168G>T ENSP00000412676.1:n.196-168G>T
NM_002775.4:c.973-168G>T NP_002766.1:n.973-168G>T
NM_002775.5:c.973-168G>T MANE Select NP_002766.1:n.973-168G>T
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