Canonical Allele Identifier: CA821639160

Gene: LPA

Linked Data

• dbSNP Id: rs1416375028
• gnomAD v3: 6-160541403-C-T
• gnomAD v4: 6-160541403-C-T
• MyVariant Identifiers: chr6:g.160962435C>T (hg19) ; chr6:g.160541403C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160541403C>T , CM000668.2:g.160541403C>T	GRCh38
NC_000006.11:g.160962435C>T , CM000668.1:g.160962435C>T	GRCh37
NC_000006.10:g.160882425C>T	NCBI36
NG_016147.1:g.129973G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.5520-222G>A MANE Select	ENSP00000321334.6:n.5520-222G>A
ENST00000316300.9:c.5520-222G>A	ENSP00000321334.5:n.5520-222G>A
NM_005577.2:c.5520-222G>A	NP_005568.2:n.5520-222G>A
NM_005577.3:c.5520-222G>A	NP_005568.2:n.5520-222G>A
NM_005577.4:c.5520-222G>A MANE Select	NP_005568.2:n.5520-222G>A