Canonical Allele Identifier: CA96760333

Gene: CWH43

Linked Data

• dbSNP Id: rs544246742
• gnomAD v3: 4-49060912-A-G
• gnomAD v4: 4-49060912-A-G
• MyVariant Identifiers: chr4:g.49062929A>G (hg19) ; chr4:g.49060912A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.49060912A>G , CM000666.2:g.49060912A>G	GRCh38
NC_000004.11:g.49062929A>G , CM000666.1:g.49062929A>G	GRCh37
NC_000004.10:g.48757686A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226432.9:c.2022-900A>G MANE Select	ENSP00000226432.4:n.2022-900A>G
ENST00000226432.8:c.2022-900A>G	ENSP00000226432.4:n.2022-900A>G
ENST00000513409.1:c.1941-900A>G	ENSP00000422802.1:n.1941-900A>G
ENST00000514053.6:c.*1032-900A>G	ENSP00000425157.2:n.*1032-900A>G
NM_001286791.1:c.1941-900A>G	NP_001273720.1:n.1941-900A>G
NM_025087.2:c.2022-900A>G	NP_079363.2:n.2022-900A>G
XM_011513755.1:c.2079-900A>G	XP_011512057.1:n.2079-900A>G
XM_011513756.1:c.1998-900A>G	XP_011512058.1:n.1998-900A>G
XM_011513757.1:c.1998-900A>G	XP_011512059.1:n.1998-900A>G
XM_011513758.1:c.1821-900A>G	XP_011512060.1:n.1821-900A>G
XM_011513759.1:c.1515-900A>G	XP_011512061.1:n.1515-900A>G
XM_011513756.3:c.1998-900A>G	XP_011512058.1:n.1998-900A>G
XM_011513757.2:c.1998-900A>G	XP_011512059.1:n.1998-900A>G
NM_025087.3:c.2022-900A>G MANE Select	NP_079363.2:n.2022-900A>G
NM_001286791.2:c.1941-900A>G	NP_001273720.1:n.1941-900A>G