Canonical Allele Identifier: CA1064325823
Gene: SHROOM3 HGNC NCBI

Linked Data

dbSNP Id: rs1731494030
gnomAD v3: 4-76476853-G-A
gnomAD v4: 4-76476853-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476853G>A , CM000666.2:g.76476853G>A GRCh38
NC_000004.11:g.77398006G>A , CM000666.1:g.77398006G>A GRCh37
NC_000004.10:g.77617030G>A NCBI36
NG_028077.1:g.46754G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296043.7:c.168+40633G>A MANE Select ENSP00000296043.6:n.168+40633G>A
ENST00000296043.6:c.168+40633G>A ENSP00000296043.6:n.168+40633G>A
ENST00000466541.1:n.75+40633G>A
ENST00000497440.5:n.109+40633G>A
NM_020859.3:c.168+40633G>A NP_065910.3:n.168+40633G>A
XM_005263162.3:c.168+40633G>A XP_005263219.1:n.168+40633G>A
XM_011532158.1:c.168+40633G>A XP_011530460.1:n.168+40633G>A
XM_011532159.1:c.168+40633G>A XP_011530461.1:n.168+40633G>A
XM_011532158.3:c.168+40633G>A XP_011530460.1:n.168+40633G>A
NM_020859.4:c.168+40633G>A MANE Select NP_065910.3:n.168+40633G>A
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