Canonical Allele Identifier: CA501476186
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224277C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228159C>G , CM000679.2:g.66228159C>G GRCh38
NC_000017.10:g.64224277C>G , CM000679.1:g.64224277C>G GRCh37
NC_000017.9:g.61654739C>G NCBI36
NG_012045.1:g.6280G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.102G>C MANE Select ENSP00000205948.6:p.Val34=
ENST00000205948.10:c.102G>C ENSP00000205948.6:p.Val34=
ENST00000577982.1:c.102G>C ENSP00000464301.1:p.Val34=
ENST00000581797.5:c.-79G>C ENSP00000463553.1:n.-79G>C
NM_000042.2:c.102G>C NP_000033.2:p.Val34=
NM_000042.3:c.102G>C MANE Select NP_000033.2:p.Val34=