Canonical Allele Identifier: CA2271191704

Gene: APOH

Linked Data

• dbSNP Id: rs2073448826

Genomic Alleles

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

Transcript Alleles

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