Canonical Allele Identifier: CA345990611
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663180294
gnomAD v4: 2-21007571-G-T
MyVariant Identifiers: chr2:g.21230443G>T (hg19) chr2:g.21007571G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007571G>T , CM000664.2:g.21007571G>T GRCh38
NC_000002.11:g.21230443G>T , CM000664.1:g.21230443G>T GRCh37
NC_000002.10:g.21083948G>T NCBI36
NG_011793.1:g.41503C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.9297C>A MANE Select ENSP00000233242.1:p.Asn3099Lys
ENST00000616098.4:c.9297C>A ENSP00000477990.1:p.Asn3099Lys
NM_000384.2:c.9297C>A NP_000375.2:p.Asn3099Lys
XM_011532809.1:c.5869+3162C>A XP_011531111.1:n.5869+3162C>A
NM_000384.3:c.9297C>A MANE Select NP_000375.3:p.Asn3099Lys
Search 100 bp 5'
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