Canonical Allele Identifier: CA400683823
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228104G>C , CM000679.2:g.66228104G>C GRCh38
NC_000017.10:g.64224222G>C , CM000679.1:g.64224222G>C GRCh37
NC_000017.9:g.61654684G>C NCBI36
NG_012045.1:g.6335C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.157C>G MANE Select ENSP00000205948.6:p.Pro53Ala
ENST00000205948.10:c.157C>G ENSP00000205948.6:p.Pro53Ala
ENST00000577982.1:c.157C>G ENSP00000464301.1:p.Pro53Ala
ENST00000581797.5:c.-24C>G ENSP00000463553.1:n.-24C>G
NM_000042.2:c.157C>G NP_000033.2:p.Pro53Ala
NM_000042.3:c.157C>G MANE Select NP_000033.2:p.Pro53Ala