Canonical Allele Identifier: CA400683974
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1433596837
gnomAD v3: 17-66228173-G-T
gnomAD v4: 17-66228173-G-T
MyVariant Identifiers: chr17:g.64224291G>T (hg19) chr17:g.66228173G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228173G>T , CM000679.2:g.66228173G>T GRCh38
NC_000017.10:g.64224291G>T , CM000679.1:g.64224291G>T GRCh37
NC_000017.9:g.61654753G>T NCBI36
NG_012045.1:g.6266C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.88C>A MANE Select ENSP00000205948.6:p.Pro30Thr
ENST00000205948.10:c.88C>A ENSP00000205948.6:p.Pro30Thr
ENST00000577982.1:c.88C>A ENSP00000464301.1:p.Pro30Thr
ENST00000581797.5:c.-93C>A ENSP00000463553.1:n.-93C>A
NM_000042.2:c.88C>A NP_000033.2:p.Pro30Thr
NM_000042.3:c.88C>A MANE Select NP_000033.2:p.Pro30Thr
Search 100 bp 5'
Search 100 bp 3'