Canonical Allele Identifier: CA400683852
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1394413014
gnomAD v2: 17-64224236-G-A
gnomAD v4: 17-66228118-G-A
MyVariant Identifiers: chr17:g.64224236G>A (hg19) chr17:g.66228118G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228118G>A , CM000679.2:g.66228118G>A GRCh38
NC_000017.10:g.64224236G>A , CM000679.1:g.64224236G>A GRCh37
NC_000017.9:g.61654698G>A NCBI36
NG_012045.1:g.6321C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.143C>T MANE Select ENSP00000205948.6:p.Thr48Met
ENST00000205948.10:c.143C>T ENSP00000205948.6:p.Thr48Met
ENST00000577982.1:c.143C>T ENSP00000464301.1:p.Thr48Met
ENST00000581797.5:c.-38C>T ENSP00000463553.1:n.-38C>T
NM_000042.2:c.143C>T NP_000033.2:p.Thr48Met
NM_000042.3:c.143C>T MANE Select NP_000033.2:p.Thr48Met
Search 100 bp 5'
Search 100 bp 3'