Canonical Allele Identifier: CA571906344
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1466968857
gnomAD v2: 6-160969747-C-G
MyVariant Identifiers: chr6:g.160969747C>G (hg19) chr6:g.160548715C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548715C>G , CM000668.2:g.160548715C>G GRCh38
NC_000006.11:g.160969747C>G , CM000668.1:g.160969747C>G GRCh37
NC_000006.10:g.160889737C>G NCBI36
NG_016147.1:g.122661G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4974-56G>C MANE Select ENSP00000321334.6:n.4974-56G>C
ENST00000316300.9:c.4974-56G>C ENSP00000321334.5:n.4974-56G>C
NM_005577.2:c.4974-56G>C NP_005568.2:n.4974-56G>C
NM_005577.3:c.4974-56G>C NP_005568.2:n.4974-56G>C
NM_005577.4:c.4974-56G>C MANE Select NP_005568.2:n.4974-56G>C
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