Canonical Allele Identifier: CA985612167
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073472576
gnomAD v3: 17-66231278-C-T
gnomAD v4: 17-66231278-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66231278C>T , CM000679.2:g.66231278C>T GRCh38
NC_000017.10:g.64227396C>T , CM000679.1:g.64227396C>T GRCh37
NC_000017.9:g.61657858C>T NCBI36
NG_012045.1:g.3161G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-1856G>A ENSP00000464301.1:n.-43-1856G>A
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