Canonical Allele Identifier: CA427813208
Gene: CNNM4 HGNC NCBI

Linked Data

gnomAD v4: 2-96761485-G-A
MyVariant Identifiers: chr2:g.97427222G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761485G>A , CM000664.2:g.96761485G>A GRCh38
NC_000002.11:g.97427222G>A , CM000664.1:g.97427222G>A GRCh37
NC_000002.10:g.96790949G>A NCBI36
NG_016608.1:g.5584G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.486G>A MANE Select ENSP00000366275.2:p.Lys162=
ENST00000377075.2:c.486G>A ENSP00000366275.2:p.Lys162=
NM_020184.3:c.486G>A NP_064569.3:p.Lys162=
XM_005263914.2:c.486G>A XP_005263971.1:p.Lys162=
XM_005263915.2:c.486G>A XP_005263972.1:p.Lys162=
XM_011510955.1:c.486G>A XP_011509257.1:p.Lys162=
XM_011510956.1:c.486G>A XP_011509258.1:p.Lys162=
XM_005263914.4:c.486G>A XP_005263971.1:p.Lys162=
XM_005263915.4:c.486G>A XP_005263972.1:p.Lys162=
XM_011510955.3:c.486G>A XP_011509257.1:p.Lys162=
XM_011510956.3:c.486G>A XP_011509258.1:p.Lys162=
NM_020184.4:c.486G>A MANE Select NP_064569.3:p.Lys162=
Search 100 bp 5'
Search 100 bp 3'