Canonical Allele Identifier: CA2576362545
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228267A>G , CM000679.2:g.66228267A>G GRCh38
NC_000017.10:g.64224385A>G , CM000679.1:g.64224385A>G GRCh37
NC_000017.9:g.61654847A>G NCBI36
NG_012045.1:g.6172T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-71T>C MANE Select ENSP00000205948.6:n.65-71T>C
ENST00000205948.10:c.65-71T>C ENSP00000205948.6:n.65-71T>C
ENST00000577982.1:c.65-71T>C ENSP00000464301.1:n.65-71T>C
ENST00000581797.5:c.-116-71T>C ENSP00000463553.1:n.-116-71T>C
NM_000042.2:c.65-71T>C NP_000033.2:n.65-71T>C
NM_000042.3:c.65-71T>C MANE Select NP_000033.2:n.65-71T>C