Canonical Allele Identifier: CA8720520
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs752002960
ExAC: 17:64224289 T / C
gnomAD v2: 17-64224289-T-C
gnomAD v4: 17-66228171-T-C
MyVariant Identifiers: chr17:g.64224289T>C (hg19) chr17:g.66228171T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228171T>C , CM000679.2:g.66228171T>C GRCh38
NC_000017.10:g.64224289T>C , CM000679.1:g.64224289T>C GRCh37
NC_000017.9:g.61654751T>C NCBI36
NG_012045.1:g.6268A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.90A>G MANE Select ENSP00000205948.6:p.Pro30=
ENST00000205948.10:c.90A>G ENSP00000205948.6:p.Pro30=
ENST00000577982.1:c.90A>G ENSP00000464301.1:p.Pro30=
ENST00000581797.5:c.-91A>G ENSP00000463553.1:n.-91A>G
NM_000042.2:c.90A>G NP_000033.2:p.Pro30=
NM_000042.3:c.90A>G MANE Select NP_000033.2:p.Pro30=
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