Canonical Allele Identifier: CA2271191913
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1598555298
gnomAD v3: 17-66228303-A-T
gnomAD v4: 17-66228303-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228303A>T , CM000679.2:g.66228303A>T GRCh38
NC_000017.10:g.64224421A>T , CM000679.1:g.64224421A>T GRCh37
NC_000017.9:g.61654883A>T NCBI36
NG_012045.1:g.6136T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-107T>A MANE Select ENSP00000205948.6:n.65-107T>A
ENST00000205948.10:c.65-107T>A ENSP00000205948.6:n.65-107T>A
ENST00000577982.1:c.65-107T>A ENSP00000464301.1:n.65-107T>A
ENST00000581797.5:c.-116-107T>A ENSP00000463553.1:n.-116-107T>A
NM_000042.2:c.65-107T>A NP_000033.2:n.65-107T>A
NM_000042.3:c.65-107T>A MANE Select NP_000033.2:n.65-107T>A
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