Canonical Allele Identifier: CA100204512

Gene: SHROOM3

Linked Data

• dbSNP Id: rs141953706
• gnomAD v3: 4-76476933-A-C
• gnomAD v4: 4-76476933-A-C
• MyVariant Identifiers: chr4:g.77398086A>C (hg19) ; chr4:g.76476933A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476933A>C , CM000666.2:g.76476933A>C	GRCh38
NC_000004.11:g.77398086A>C , CM000666.1:g.77398086A>C	GRCh37
NC_000004.10:g.77617110A>C	NCBI36
NG_028077.1:g.46834A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.168+40713A>C MANE Select	ENSP00000296043.6:n.168+40713A>C
ENST00000296043.6:c.168+40713A>C	ENSP00000296043.6:n.168+40713A>C
ENST00000466541.1:n.75+40713A>C
ENST00000497440.5:n.109+40713A>C
NM_020859.3:c.168+40713A>C	NP_065910.3:n.168+40713A>C
XM_005263162.3:c.168+40713A>C	XP_005263219.1:n.168+40713A>C
XM_011532158.1:c.168+40713A>C	XP_011530460.1:n.168+40713A>C
XM_011532159.1:c.168+40713A>C	XP_011530461.1:n.168+40713A>C
XM_011532158.3:c.168+40713A>C	XP_011530460.1:n.168+40713A>C
NM_020859.4:c.168+40713A>C MANE Select	NP_065910.3:n.168+40713A>C