Canonical Allele Identifier: CA16543774

Gene: APOH

Linked Data

• dbSNP Id: rs545554785
• gnomAD v2: 17-64224034-A-G
• gnomAD v3: 17-66227916-A-G
• gnomAD v4: 17-66227916-A-G
• MyVariant Identifiers: chr17:g.64224034A>G (hg19) ; chr17:g.66227916A>G (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66227916A>G , CM000679.2:g.66227916A>G	GRCh38
NC_000017.10:g.64224034A>G , CM000679.1:g.64224034A>G	GRCh37
NC_000017.9:g.61654496A>G	NCBI36
NG_012045.1:g.6523T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.241+104T>C MANE Select	ENSP00000205948.6:n.241+104T>C
ENST00000205948.10:c.241+104T>C	ENSP00000205948.6:n.241+104T>C
ENST00000577982.1:c.241+104T>C	ENSP00000464301.1:n.241+104T>C
ENST00000581797.5:c.61+104T>C	ENSP00000463553.1:n.61+104T>C
NM_000042.2:c.241+104T>C	NP_000033.2:n.241+104T>C
NM_000042.3:c.241+104T>C MANE Select	NP_000033.2:n.241+104T>C