Canonical Allele Identifier: CA293118544
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs913427021
gnomAD v4: 17-66228281-T-C
MyVariant Identifiers: chr17:g.64224399T>C (hg19) chr17:g.66228281T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228281T>C , CM000679.2:g.66228281T>C GRCh38
NC_000017.10:g.64224399T>C , CM000679.1:g.64224399T>C GRCh37
NC_000017.9:g.61654861T>C NCBI36
NG_012045.1:g.6158A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-85A>G MANE Select ENSP00000205948.6:n.65-85A>G
ENST00000205948.10:c.65-85A>G ENSP00000205948.6:n.65-85A>G
ENST00000577982.1:c.65-85A>G ENSP00000464301.1:n.65-85A>G
ENST00000581797.5:c.-116-85A>G ENSP00000463553.1:n.-116-85A>G
NM_000042.2:c.65-85A>G NP_000033.2:n.65-85A>G
NM_000042.3:c.65-85A>G MANE Select NP_000033.2:n.65-85A>G
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