Canonical Allele Identifier: CA774231596
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1411903368
gnomAD v3: 17-66228273-A-C
gnomAD v4: 17-66228273-A-C
MyVariant Identifiers: chr17:g.64224391A>C (hg19) chr17:g.66228273A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228273A>C , CM000679.2:g.66228273A>C GRCh38
NC_000017.10:g.64224391A>C , CM000679.1:g.64224391A>C GRCh37
NC_000017.9:g.61654853A>C NCBI36
NG_012045.1:g.6166T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-77T>G MANE Select ENSP00000205948.6:n.65-77T>G
ENST00000205948.10:c.65-77T>G ENSP00000205948.6:n.65-77T>G
ENST00000577982.1:c.65-77T>G ENSP00000464301.1:n.65-77T>G
ENST00000581797.5:c.-116-77T>G ENSP00000463553.1:n.-116-77T>G
NM_000042.2:c.65-77T>G NP_000033.2:n.65-77T>G
NM_000042.3:c.65-77T>G MANE Select NP_000033.2:n.65-77T>G
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