Canonical Allele Identifier: CA2271191735
Gene: APOH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227920A= , CM000679.2:g.66227920A= GRCh38
NC_000017.10:g.64224038A= , CM000679.1:g.64224038A= GRCh37
NC_000017.9:g.61654500A= NCBI36
NG_012045.1:g.6519T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+100T= MANE Select ENSP00000205948.6:n.241+100T=
ENST00000205948.10:c.241+100T= ENSP00000205948.6:n.241+100T=
ENST00000577982.1:c.241+100T= ENSP00000464301.1:n.241+100T=
ENST00000581797.5:c.61+100T= ENSP00000463553.1:n.61+100T=
NM_000042.2:c.241+100T= NP_000033.2:n.241+100T=
NM_000042.3:c.241+100T= MANE Select NP_000033.2:n.241+100T=
Search 100 bp 5'
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