Canonical Allele Identifier: CA774231569
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1258283781
gnomAD v3: 17-66228233-C-G
gnomAD v4: 17-66228233-C-G
MyVariant Identifiers: chr17:g.64224351C>G (hg19) chr17:g.66228233C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228233C>G , CM000679.2:g.66228233C>G GRCh38
NC_000017.10:g.64224351C>G , CM000679.1:g.64224351C>G GRCh37
NC_000017.9:g.61654813C>G NCBI36
NG_012045.1:g.6206G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-37G>C MANE Select ENSP00000205948.6:n.65-37G>C
ENST00000205948.10:c.65-37G>C ENSP00000205948.6:n.65-37G>C
ENST00000577982.1:c.65-37G>C ENSP00000464301.1:n.65-37G>C
ENST00000581797.5:c.-116-37G>C ENSP00000463553.1:n.-116-37G>C
NM_000042.2:c.65-37G>C NP_000033.2:n.65-37G>C
NM_000042.3:c.65-37G>C MANE Select NP_000033.2:n.65-37G>C
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