Canonical Allele Identifier: CA11650848
Gene: SHROOM3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10032549

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476862A>G , CM000666.2:g.76476862A>G GRCh38
NC_000004.11:g.77398015A>G , CM000666.1:g.77398015A>G GRCh37
NC_000004.10:g.77617039A>G NCBI36
NG_028077.1:g.46763A>G

Transcript Alleles

HGVS Amino-acid change
NM_020859.3:c.168+40642A>G VV NP_065910.3:p.=
XM_005263162.3:c.168+40642A>G XP_005263219.1:p.=
XM_011532158.1:c.168+40642A>G XP_011530460.1:p.=
XM_011532159.1:c.168+40642A>G XP_011530461.1:p.=
XM_011532158.3:c.168+40642A>G
NM_020859.4:c.168+40642A>G VV MANE Preferred
ENST00000296043.6:c.168+40642A>G ENSP00000296043.6:p.=
ENST00000466541.1:n.75+40642A>G
ENST00000497440.5:n.109+40642A>G