Canonical Allele Identifier: CA4087775
Gene: PLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2777133
ClinVar RCV Id: RCV003665143
dbSNP Id: rs1333528760
ExAC: 6:161152244 T / C
gnomAD v2: 6-161152244-T-C
gnomAD v3: 6-160731212-T-C
gnomAD v4: 6-160731212-T-C
MyVariant Identifiers: chr6:g.161152244T>C (hg19) chr6:g.161152244_161152246delinsCAG (hg19) chr6:g.160731212T>C (hg38) chr6:g.160731212_160731214delinsCAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160731212T>C , CM000668.2:g.160731212T>C GRCh38
NC_000006.11:g.161152244T>C , CM000668.1:g.161152244T>C GRCh37
NC_000006.10:g.161072234T>C NCBI36
NG_016200.1:g.34020T>C , LRG_571:g.34020T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.371T>C ENSP00000516619.1:p.Val124Ala
ENST00000418964.2:c.1469T>C ENSP00000389424.2:p.Val490Ala
ENST00000706906.1:c.1418T>C ENSP00000516618.1:p.Val473Ala
ENST00000308192.14:c.1418T>C MANE Select ENSP00000308938.9:p.Val473Ala
ENST00000297289.8:n.416T>C
ENST00000308192.13:c.1418T>C ENSP00000308938.9:p.Val473Ala
ENST00000493435.1:n.473T>C
NM_000301.3:c.1418T>C , LRG_571t1:c.1418T>C NP_000292.1:p.Val473Ala
NM_000301.4:c.1418T>C NP_000292.1:p.Val473Ala
NM_000301.5:c.1418T>C MANE Select NP_000292.1:p.Val473Ala
Search 100 bp 5'
Search 100 bp 3'