Canonical Allele Identifier: CA425344155
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21230074G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007202G>C , CM000664.2:g.21007202G>C GRCh38
NC_000002.11:g.21230074G>C , CM000664.1:g.21230074G>C GRCh37
NC_000002.10:g.21083579G>C NCBI36
NG_011793.1:g.41872C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.9666C>G MANE Select ENSP00000233242.1:p.Ser3222=
ENST00000616098.4:c.9666C>G ENSP00000477990.1:p.Ser3222=
NM_000384.2:c.9666C>G NP_000375.2:p.Ser3222=
XM_011532809.1:c.5869+3531C>G XP_011531111.1:n.5869+3531C>G
NM_000384.3:c.9666C>G MANE Select NP_000375.3:p.Ser3222=
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