Canonical Allele Identifier: CA626911831
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1481791225
gnomAD v2: 17-64223988-A-T
gnomAD v3: 17-66227870-A-T
gnomAD v4: 17-66227870-A-T
MyVariant Identifiers: chr17:g.64223988A>T (hg19) chr17:g.66227870A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227870A>T , CM000679.2:g.66227870A>T GRCh38
NC_000017.10:g.64223988A>T , CM000679.1:g.64223988A>T GRCh37
NC_000017.9:g.61654450A>T NCBI36
NG_012045.1:g.6569T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+150T>A MANE Select ENSP00000205948.6:n.241+150T>A
ENST00000205948.10:c.241+150T>A ENSP00000205948.6:n.241+150T>A
ENST00000577982.1:c.241+150T>A ENSP00000464301.1:n.241+150T>A
ENST00000581797.5:c.61+150T>A ENSP00000463553.1:n.61+150T>A
NM_000042.2:c.241+150T>A NP_000033.2:n.241+150T>A
NM_000042.3:c.241+150T>A MANE Select NP_000033.2:n.241+150T>A
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