Canonical Allele Identifier: CA2611238774
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461595-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461595G>C , CM000672.2:g.122461595G>C GRCh38
NC_000010.10:g.124221111G>C , CM000672.1:g.124221111G>C GRCh37
NC_000010.9:g.124211101G>C NCBI36
NG_011554.1:g.5071G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.-58G>C MANE Select ENSP00000357980.3:n.-58G>C
ENST00000648167.1:c.154+2886G>C ENSP00000498033.1:n.154+2886G>C
ENST00000368984.7:c.-58G>C ENSP00000357980.3:n.-58G>C
NM_002775.4:c.-58G>C NP_002766.1:n.-58G>C
NM_002775.5:c.-58G>C MANE Select NP_002766.1:n.-58G>C
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