Canonical Allele Identifier: CA64347072
Gene: PARD3B HGNC NCBI

Linked Data

dbSNP Id: rs11884476

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.205453869C>G , CM000664.2:g.205453869C>G GRCh38
NC_000002.11:g.206318593C>G , CM000664.1:g.206318593C>G GRCh37
NC_000002.10:g.206026838C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406610.7:c.3044+13197C>G MANE Select ENSP00000385848.2:n.3044+13197C>G
ENST00000349953.7:c.2742-46027C>G ENSP00000340280.3:n.2742-46027C>G
ENST00000351153.5:c.2837+13197C>G ENSP00000317261.2:n.2837+13197C>G
ENST00000358768.6:c.2858+13197C>G ENSP00000351618.2:n.2858+13197C>G
ENST00000406610.6:c.3044+13197C>G ENSP00000385848.2:n.3044+13197C>G
ENST00000613457.4:c.2636+13197C>G ENSP00000484434.1:n.2636+13197C>G
ENST00000614500.3:c.2615+13197C>G ENSP00000481918.1:n.2615+13197C>G
ENST00000622699.2:c.2520-46027C>G ENSP00000482649.1:n.2520-46027C>G
NM_001302769.1:c.3044+13197C>G NP_001289698.1:n.3044+13197C>G
NM_057177.6:c.2837+13197C>G NP_476518.4:n.2837+13197C>G
NM_152526.5:c.2858+13197C>G NP_689739.4:n.2858+13197C>G
NM_205863.3:c.2742-46027C>G NP_995585.2:n.2742-46027C>G
XM_011510550.1:c.3104+13197C>G XP_011508852.1:n.3104+13197C>G
XM_011510551.1:c.3044+13197C>G XP_011508853.1:n.3044+13197C>G
XM_011510552.1:c.3068+13197C>G XP_011508854.1:n.3068+13197C>G
XM_011510552.2:c.3068+13197C>G XP_011508854.1:n.3068+13197C>G
XM_017003283.1:c.3008+13197C>G XP_016858772.1:n.3008+13197C>G
XM_017003284.1:c.2978+13197C>G XP_016858773.1:n.2978+13197C>G
XM_017003285.1:c.2882+13197C>G XP_016858774.1:n.2882+13197C>G
XM_017003286.1:c.2876+13197C>G XP_016858775.1:n.2876+13197C>G
XM_017003287.1:c.3068+13197C>G XP_016858776.1:n.3068+13197C>G
XM_017003288.1:c.2766-46027C>G XP_016858777.1:n.2766-46027C>G
XM_017003289.1:c.2543+13197C>G XP_016858778.1:n.2543+13197C>G
XM_017003290.1:c.2447+13197C>G XP_016858779.1:n.2447+13197C>G
XM_017003291.1:c.2447+13197C>G XP_016858780.1:n.2447+13197C>G
XM_017003292.1:c.2447+13197C>G XP_016858781.1:n.2447+13197C>G
XM_017003293.1:c.2447+13197C>G XP_016858782.1:n.2447+13197C>G
NM_001302769.2:c.3044+13197C>G MANE Select NP_001289698.1:n.3044+13197C>G
NM_057177.7:c.2837+13197C>G NP_476518.4:n.2837+13197C>G
NM_152526.6:c.2858+13197C>G NP_689739.4:n.2858+13197C>G
NM_205863.4:c.2742-46027C>G NP_995585.2:n.2742-46027C>G