Canonical Allele Identifier: CA427813442

Gene: CNNM4

Linked Data

• gnomAD v4: 2-96761662-C-A
• MyVariant Identifiers: chr2:g.97427399C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761662C>A , CM000664.2:g.96761662C>A	GRCh38
NC_000002.11:g.97427399C>A , CM000664.1:g.97427399C>A	GRCh37
NC_000002.10:g.96791126C>A	NCBI36
NG_016608.1:g.5761C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.663C>A MANE Select	ENSP00000366275.2:p.Gly221=
ENST00000377075.2:c.663C>A	ENSP00000366275.2:p.Gly221=
NM_020184.3:c.663C>A	NP_064569.3:p.Gly221=
XM_005263914.2:c.663C>A	XP_005263971.1:p.Gly221=
XM_005263915.2:c.663C>A	XP_005263972.1:p.Gly221=
XM_011510955.1:c.663C>A	XP_011509257.1:p.Gly221=
XM_011510956.1:c.663C>A	XP_011509258.1:p.Gly221=
XM_005263914.4:c.663C>A	XP_005263971.1:p.Gly221=
XM_005263915.4:c.663C>A	XP_005263972.1:p.Gly221=
XM_011510955.3:c.663C>A	XP_011509257.1:p.Gly221=
XM_011510956.3:c.663C>A	XP_011509258.1:p.Gly221=
NM_020184.4:c.663C>A MANE Select	NP_064569.3:p.Gly221=