Canonical Allele Identifier: CA501476165
Gene: APOH HGNC NCBI

Linked Data

gnomAD v4: 17-66228144-T-C
MyVariant Identifiers: chr17:g.64224262T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228144T>C , CM000679.2:g.66228144T>C GRCh38
NC_000017.10:g.64224262T>C , CM000679.1:g.64224262T>C GRCh37
NC_000017.9:g.61654724T>C NCBI36
NG_012045.1:g.6295A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.117A>G MANE Select ENSP00000205948.6:p.Thr39=
ENST00000205948.10:c.117A>G ENSP00000205948.6:p.Thr39=
ENST00000577982.1:c.117A>G ENSP00000464301.1:p.Thr39=
ENST00000581797.5:c.-64A>G ENSP00000463553.1:n.-64A>G
NM_000042.2:c.117A>G NP_000033.2:p.Thr39=
NM_000042.3:c.117A>G MANE Select NP_000033.2:p.Thr39=
Search 100 bp 5'
Search 100 bp 3'