Canonical Allele Identifier: CA347713665

Gene: CNNM4

Linked Data

• dbSNP Id: rs1189944514
• gnomAD v2: 2-97427155-G-A
• gnomAD v4: 2-96761418-G-A
• MyVariant Identifiers: chr2:g.97427155G>A (hg19) ; chr2:g.96761418G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761418G>A , CM000664.2:g.96761418G>A	GRCh38
NC_000002.11:g.97427155G>A , CM000664.1:g.97427155G>A	GRCh37
NC_000002.10:g.96790882G>A	NCBI36
NG_016608.1:g.5517G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.419G>A MANE Select	ENSP00000366275.2:p.Arg140Gln
ENST00000377075.2:c.419G>A	ENSP00000366275.2:p.Arg140Gln
NM_020184.3:c.419G>A	NP_064569.3:p.Arg140Gln
XM_005263914.2:c.419G>A	XP_005263971.1:p.Arg140Gln
XM_005263915.2:c.419G>A	XP_005263972.1:p.Arg140Gln
XM_011510955.1:c.419G>A	XP_011509257.1:p.Arg140Gln
XM_011510956.1:c.419G>A	XP_011509258.1:p.Arg140Gln
XM_005263914.4:c.419G>A	XP_005263971.1:p.Arg140Gln
XM_005263915.4:c.419G>A	XP_005263972.1:p.Arg140Gln
XM_011510955.3:c.419G>A	XP_011509257.1:p.Arg140Gln
XM_011510956.3:c.419G>A	XP_011509258.1:p.Arg140Gln
NM_020184.4:c.419G>A MANE Select	NP_064569.3:p.Arg140Gln