Canonical Allele Identifier: CA2271191703
Gene: APOH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227858T= , CM000679.2:g.66227858T= GRCh38
NC_000017.10:g.64223976T= , CM000679.1:g.64223976T= GRCh37
NC_000017.9:g.61654438T= NCBI36
NG_012045.1:g.6581A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+162A= MANE Select ENSP00000205948.6:n.241+162A=
ENST00000205948.10:c.241+162A= ENSP00000205948.6:n.241+162A=
ENST00000577982.1:c.241+162A= ENSP00000464301.1:n.241+162A=
ENST00000581797.5:c.61+162A= ENSP00000463553.1:n.61+162A=
NM_000042.2:c.241+162A= NP_000033.2:n.241+162A=
NM_000042.3:c.241+162A= MANE Select NP_000033.2:n.241+162A=
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