Canonical Allele Identifier: CA501476181
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224274G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228156G>T , CM000679.2:g.66228156G>T GRCh38
NC_000017.10:g.64224274G>T , CM000679.1:g.64224274G>T GRCh37
NC_000017.9:g.61654736G>T NCBI36
NG_012045.1:g.6283C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.105C>A MANE Select ENSP00000205948.6:p.Val35=
ENST00000205948.10:c.105C>A ENSP00000205948.6:p.Val35=
ENST00000577982.1:c.105C>A ENSP00000464301.1:p.Val35=
ENST00000581797.5:c.-76C>A ENSP00000463553.1:n.-76C>A
NM_000042.2:c.105C>A NP_000033.2:p.Val35=
NM_000042.3:c.105C>A MANE Select NP_000033.2:p.Val35=