Canonical Allele Identifier: CA8720528
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs771121736
ExAC: 17:64224349 C / A
gnomAD v2: 17-64224349-C-A
gnomAD v4: 17-66228231-C-A
MyVariant Identifiers: chr17:g.64224349C>A (hg19) chr17:g.66228231C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228231C>A , CM000679.2:g.66228231C>A GRCh38
NC_000017.10:g.64224349C>A , CM000679.1:g.64224349C>A GRCh37
NC_000017.9:g.61654811C>A NCBI36
NG_012045.1:g.6208G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-35G>T MANE Select ENSP00000205948.6:n.65-35G>T
ENST00000205948.10:c.65-35G>T ENSP00000205948.6:n.65-35G>T
ENST00000577982.1:c.65-35G>T ENSP00000464301.1:n.65-35G>T
ENST00000581797.5:c.-116-35G>T ENSP00000463553.1:n.-116-35G>T
NM_000042.2:c.65-35G>T NP_000033.2:n.65-35G>T
NM_000042.3:c.65-35G>T MANE Select NP_000033.2:n.65-35G>T
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