Canonical Allele Identifier: CA16124373

Gene: PARD3B

Linked Data

• dbSNP Id: rs849230
• gnomAD v2: 2-206261029-G-A
• gnomAD v3: 2-205396305-G-A
• gnomAD v4: 2-205396305-G-A
• MyVariant Identifiers: chr2:g.206261029G>A (hg19) ; chr2:g.205396305G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.205396305G>A , CM000664.2:g.205396305G>A	GRCh38
NC_000002.11:g.206261029G>A , CM000664.1:g.206261029G>A	GRCh37
NC_000002.10:g.205969274G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406610.7:c.2631-4708G>A MANE Select	ENSP00000385848.2:n.2631-4708G>A
ENST00000349953.7:c.2631-4708G>A	ENSP00000340280.3:n.2631-4708G>A
ENST00000351153.5:c.2424-4708G>A	ENSP00000317261.2:n.2424-4708G>A
ENST00000358768.6:c.2445-4708G>A	ENSP00000351618.2:n.2445-4708G>A
ENST00000406610.6:c.2631-4708G>A	ENSP00000385848.2:n.2631-4708G>A
ENST00000494482.1:n.364-4708G>A
ENST00000613457.4:c.2223-4708G>A	ENSP00000484434.1:n.2223-4708G>A
ENST00000614500.3:c.2202-4708G>A	ENSP00000481918.1:n.2202-4708G>A
ENST00000622699.2:c.2409-4708G>A	ENSP00000482649.1:n.2409-4708G>A
NM_001302769.1:c.2631-4708G>A	NP_001289698.1:n.2631-4708G>A
NM_057177.6:c.2424-4708G>A	NP_476518.4:n.2424-4708G>A
NM_152526.5:c.2445-4708G>A	NP_689739.4:n.2445-4708G>A
NM_205863.3:c.2631-4708G>A	NP_995585.2:n.2631-4708G>A
XM_011510550.1:c.2691-4708G>A	XP_011508852.1:n.2691-4708G>A
XM_011510551.1:c.2631-4708G>A	XP_011508853.1:n.2631-4708G>A
XM_011510552.1:c.2655-4708G>A	XP_011508854.1:n.2655-4708G>A
XM_011510552.2:c.2655-4708G>A	XP_011508854.1:n.2655-4708G>A
XM_017003283.1:c.2595-4708G>A	XP_016858772.1:n.2595-4708G>A
XM_017003284.1:c.2565-4708G>A	XP_016858773.1:n.2565-4708G>A
XM_017003285.1:c.2469-4708G>A	XP_016858774.1:n.2469-4708G>A
XM_017003286.1:c.2463-4708G>A	XP_016858775.1:n.2463-4708G>A
XM_017003287.1:c.2655-4708G>A	XP_016858776.1:n.2655-4708G>A
XM_017003288.1:c.2655-4708G>A	XP_016858777.1:n.2655-4708G>A
XM_017003289.1:c.2130-4708G>A	XP_016858778.1:n.2130-4708G>A
XM_017003290.1:c.2034-4708G>A	XP_016858779.1:n.2034-4708G>A
XM_017003291.1:c.2034-4708G>A	XP_016858780.1:n.2034-4708G>A
XM_017003292.1:c.2034-4708G>A	XP_016858781.1:n.2034-4708G>A
XM_017003293.1:c.2034-4708G>A	XP_016858782.1:n.2034-4708G>A
NM_001302769.2:c.2631-4708G>A MANE Select	NP_001289698.1:n.2631-4708G>A
NM_057177.7:c.2424-4708G>A	NP_476518.4:n.2424-4708G>A
NM_152526.6:c.2445-4708G>A	NP_689739.4:n.2445-4708G>A
NM_205863.4:c.2631-4708G>A	NP_995585.2:n.2631-4708G>A