Canonical Allele Identifier: CA366364784
Gene: PLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.161157918G>C (hg19) chr6:g.160736886G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160736886G>C , CM000668.2:g.160736886G>C GRCh38
NC_000006.11:g.161157918G>C , CM000668.1:g.161157918G>C GRCh37
NC_000006.10:g.161077908G>C NCBI36
NG_016200.1:g.39694G>C , LRG_571:g.39694G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.635-1G>C ENSP00000516619.1:n.635-1G>C
ENST00000418964.2:c.1733-1G>C ENSP00000389424.2:n.1733-1G>C
ENST00000706906.1:c.*1701G>C ENSP00000516618.1:n.*1701G>C
ENST00000308192.14:c.1682-1G>C MANE Select ENSP00000308938.9:n.1682-1G>C
ENST00000308192.13:c.1682-1G>C ENSP00000308938.9:n.1682-1G>C
NM_000301.3:c.1682-1G>C , LRG_571t1:c.1682-1G>C NP_000292.1:n.1682-1G>C
NM_000301.4:c.1682-1G>C NP_000292.1:n.1682-1G>C
NM_000301.5:c.1682-1G>C MANE Select NP_000292.1:n.1682-1G>C
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