Canonical Allele Identifier: CA571551894

Gene: PLG

Linked Data

• dbSNP Id: rs1023952165
• gnomAD v2: 6-161162465-T-G
• gnomAD v4: 6-160741433-T-G
• MyVariant Identifiers: chr6:g.161162465T>G (hg19) ; chr6:g.160741433T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741433T>G , CM000668.2:g.160741433T>G	GRCh38
NC_000006.11:g.161162465T>G , CM000668.1:g.161162465T>G	GRCh37
NC_000006.10:g.161082455T>G	NCBI36
NG_016200.1:g.44241T>G , LRG_571:g.44241T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+16T>G	ENSP00000516619.1:n.1078+16T>G
ENST00000418964.2:c.2176+16T>G	ENSP00000389424.2:n.2176+16T>G
ENST00000706906.1:c.*2145+16T>G	ENSP00000516618.1:n.*2145+16T>G
ENST00000308192.14:c.2125+16T>G MANE Select	ENSP00000308938.9:n.2125+16T>G
ENST00000308192.13:c.2125+16T>G	ENSP00000308938.9:n.2125+16T>G
ENST00000461414.2:n.99+65T>G
ENST00000467466.1:n.426+16T>G
NM_000301.3:c.2125+16T>G , LRG_571t1:c.2125+16T>G	NP_000292.1:n.2125+16T>G
NM_000301.4:c.2125+16T>G	NP_000292.1:n.2125+16T>G
NM_000301.5:c.2125+16T>G MANE Select	NP_000292.1:n.2125+16T>G