Canonical Allele Identifier: CA151220216

Gene: LPA

Linked Data

• dbSNP Id: rs959696558
• MyVariant Identifiers: chr6:g.160962514C>G (hg19) ; chr6:g.160541482C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160541482C>G , CM000668.2:g.160541482C>G	GRCh38
NC_000006.11:g.160962514C>G , CM000668.1:g.160962514C>G	GRCh37
NC_000006.10:g.160882504C>G	NCBI36
NG_016147.1:g.129894G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.5520-301G>C MANE Select	ENSP00000321334.6:n.5520-301G>C
ENST00000316300.9:c.5520-301G>C	ENSP00000321334.5:n.5520-301G>C
NM_005577.2:c.5520-301G>C	NP_005568.2:n.5520-301G>C
NM_005577.3:c.5520-301G>C	NP_005568.2:n.5520-301G>C
NM_005577.4:c.5520-301G>C MANE Select	NP_005568.2:n.5520-301G>C