Canonical Allele Identifier: CA1469632621
Gene: SHROOM3 HGNC NCBI

Linked Data

dbSNP Id: rs1731492573
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76476749T>C , CM000666.2:g.76476749T>C GRCh38
NC_000004.11:g.77397902T>C , CM000666.1:g.77397902T>C GRCh37
NC_000004.10:g.77616926T>C NCBI36
NG_028077.1:g.46650T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296043.7:c.168+40529T>C MANE Select ENSP00000296043.6:n.168+40529T>C
ENST00000296043.6:c.168+40529T>C ENSP00000296043.6:n.168+40529T>C
ENST00000466541.1:n.75+40529T>C
ENST00000497440.5:n.109+40529T>C
NM_020859.3:c.168+40529T>C NP_065910.3:n.168+40529T>C
XM_005263162.3:c.168+40529T>C XP_005263219.1:n.168+40529T>C
XM_011532158.1:c.168+40529T>C XP_011530460.1:n.168+40529T>C
XM_011532159.1:c.168+40529T>C XP_011530461.1:n.168+40529T>C
XM_011532158.3:c.168+40529T>C XP_011530460.1:n.168+40529T>C
NM_020859.4:c.168+40529T>C MANE Select NP_065910.3:n.168+40529T>C
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