Canonical Allele Identifier: CA2271191701
Gene: APOH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227856T= , CM000679.2:g.66227856T= GRCh38
NC_000017.10:g.64223974T= , CM000679.1:g.64223974T= GRCh37
NC_000017.9:g.61654436T= NCBI36
NG_012045.1:g.6583A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+164A= MANE Select ENSP00000205948.6:n.241+164A=
ENST00000205948.10:c.241+164A= ENSP00000205948.6:n.241+164A=
ENST00000577982.1:c.241+164A= ENSP00000464301.1:n.241+164A=
ENST00000581797.5:c.61+164A= ENSP00000463553.1:n.61+164A=
NM_000042.2:c.241+164A= NP_000033.2:n.241+164A=
NM_000042.3:c.241+164A= MANE Select NP_000033.2:n.241+164A=
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