Canonical Allele Identifier: CA100204503

Gene: SHROOM3

Linked Data

• dbSNP Id: rs140098384
• gnomAD v2: 4-77397964-A-G
• gnomAD v3: 4-76476811-A-G
• gnomAD v4: 4-76476811-A-G
• MyVariant Identifiers: chr4:g.77397964A>G (hg19) ; chr4:g.76476811A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476811A>G , CM000666.2:g.76476811A>G	GRCh38
NC_000004.11:g.77397964A>G , CM000666.1:g.77397964A>G	GRCh37
NC_000004.10:g.77616988A>G	NCBI36
NG_028077.1:g.46712A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40591A>G MANE Select	ENSP00000296043.6:n.168+40591A>G
ENST00000296043.6:c.168+40591A>G	ENSP00000296043.6:n.168+40591A>G
ENST00000466541.1:n.75+40591A>G
ENST00000497440.5:n.109+40591A>G
NM_020859.3:c.168+40591A>G	NP_065910.3:n.168+40591A>G
XM_005263162.3:c.168+40591A>G	XP_005263219.1:n.168+40591A>G
XM_011532158.1:c.168+40591A>G	XP_011530460.1:n.168+40591A>G
XM_011532159.1:c.168+40591A>G	XP_011530461.1:n.168+40591A>G
XM_011532158.3:c.168+40591A>G	XP_011530460.1:n.168+40591A>G
NM_020859.4:c.168+40591A>G MANE Select	NP_065910.3:n.168+40591A>G