Canonical Allele Identifier: CA293118548
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs978903696
gnomAD v3: 17-66228307-A-G
gnomAD v4: 17-66228307-A-G
MyVariant Identifiers: chr17:g.64224425A>G (hg19) chr17:g.66228307A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228307A>G , CM000679.2:g.66228307A>G GRCh38
NC_000017.10:g.64224425A>G , CM000679.1:g.64224425A>G GRCh37
NC_000017.9:g.61654887A>G NCBI36
NG_012045.1:g.6132T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-111T>C MANE Select ENSP00000205948.6:n.65-111T>C
ENST00000205948.10:c.65-111T>C ENSP00000205948.6:n.65-111T>C
ENST00000577982.1:c.65-111T>C ENSP00000464301.1:n.65-111T>C
ENST00000581797.5:c.-116-111T>C ENSP00000463553.1:n.-116-111T>C
NM_000042.2:c.65-111T>C NP_000033.2:n.65-111T>C
NM_000042.3:c.65-111T>C MANE Select NP_000033.2:n.65-111T>C
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