Canonical Allele Identifier: CA501476138
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1466347473
gnomAD v2: 17-64224229-G-A
gnomAD v4: 17-66228111-G-A
MyVariant Identifiers: chr17:g.64224229G>A (hg19) chr17:g.66228111G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228111G>A , CM000679.2:g.66228111G>A GRCh38
NC_000017.10:g.64224229G>A , CM000679.1:g.64224229G>A GRCh37
NC_000017.9:g.61654691G>A NCBI36
NG_012045.1:g.6328C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.150C>T MANE Select ENSP00000205948.6:p.Ser50=
ENST00000205948.10:c.150C>T ENSP00000205948.6:p.Ser50=
ENST00000577982.1:c.150C>T ENSP00000464301.1:p.Ser50=
ENST00000581797.5:c.-31C>T ENSP00000463553.1:n.-31C>T
NM_000042.2:c.150C>T NP_000033.2:p.Ser50=
NM_000042.3:c.150C>T MANE Select NP_000033.2:p.Ser50=
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