Canonical Allele Identifier: CA821639198
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1349584515
gnomAD v3: 6-160541488-C-A
gnomAD v4: 6-160541488-C-A
MyVariant Identifiers: chr6:g.160962520C>A (hg19) chr6:g.160541488C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541488C>A , CM000668.2:g.160541488C>A GRCh38
NC_000006.11:g.160962520C>A , CM000668.1:g.160962520C>A GRCh37
NC_000006.10:g.160882510C>A NCBI36
NG_016147.1:g.129888G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5520-307G>T MANE Select ENSP00000321334.6:n.5520-307G>T
ENST00000316300.9:c.5520-307G>T ENSP00000321334.5:n.5520-307G>T
NM_005577.2:c.5520-307G>T NP_005568.2:n.5520-307G>T
NM_005577.3:c.5520-307G>T NP_005568.2:n.5520-307G>T
NM_005577.4:c.5520-307G>T MANE Select NP_005568.2:n.5520-307G>T
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