Canonical Allele Identifier: CA293118545
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs925959966
gnomAD v3: 17-66228285-G-C
gnomAD v4: 17-66228285-G-C
MyVariant Identifiers: chr17:g.64224403G>C (hg19) chr17:g.66228285G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228285G>C , CM000679.2:g.66228285G>C GRCh38
NC_000017.10:g.64224403G>C , CM000679.1:g.64224403G>C GRCh37
NC_000017.9:g.61654865G>C NCBI36
NG_012045.1:g.6154C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-89C>G MANE Select ENSP00000205948.6:n.65-89C>G
ENST00000205948.10:c.65-89C>G ENSP00000205948.6:n.65-89C>G
ENST00000577982.1:c.65-89C>G ENSP00000464301.1:n.65-89C>G
ENST00000581797.5:c.-116-89C>G ENSP00000463553.1:n.-116-89C>G
NM_000042.2:c.65-89C>G NP_000033.2:n.65-89C>G
NM_000042.3:c.65-89C>G MANE Select NP_000033.2:n.65-89C>G
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