Canonical Allele Identifier: CA8720522
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs775600856
ExAC: 17:64224317 GA / G
gnomAD v2: 17-64224317-GA-G
gnomAD v4: 17-66228199-GA-G
MyVariant Identifiers: chr17:g.64224318del (hg19) chr17:g.66228200del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228202del , CM000679.2:g.66228202del GRCh38
NC_000017.10:g.64224320del , CM000679.1:g.64224320del GRCh37
NC_000017.9:g.61654782del NCBI36
NG_012045.1:g.6239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-4del MANE Select ENSP00000205948.6:n.65-4del
ENST00000205948.10:c.65-4del ENSP00000205948.6:n.65-4del
ENST00000577982.1:c.65-4del ENSP00000464301.1:n.65-4del
ENST00000581797.5:c.-116-4del ENSP00000463553.1:n.-116-4del
NM_000042.2:c.65-4del NP_000033.2:n.65-4del
NM_000042.3:c.65-4del MANE Select NP_000033.2:n.65-4del
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