Canonical Allele Identifier: CA762866751

Gene: HECW2

Linked Data

• dbSNP Id: rs1169835918
• gnomAD v3: 2-196216979-A-C
• gnomAD v4: 2-196216979-A-C
• MyVariant Identifiers: chr2:g.197081703A>C (hg19) ; chr2:g.196216979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.196216979A>C , CM000664.2:g.196216979A>C	GRCh38
NC_000002.11:g.197081703A>C , CM000664.1:g.197081703A>C	GRCh37
NC_000002.10:g.196789948A>C	NCBI36
NG_053156.1:g.381714T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260983.8:c.4494+29T>G	ENSP00000260983.2:n.4494+29T>G
ENST00000642318.1:n.1252+29T>G
ENST00000644030.1:c.4515+29T>G	ENSP00000495504.1:n.4515+29T>G
ENST00000644256.1:c.4494+29T>G	ENSP00000494649.1:n.4494+29T>G
ENST00000644421.1:c.2218+29T>G
ENST00000644978.2:c.4494+29T>G MANE Select	ENSP00000495418.1:n.4494+29T>G
ENST00000647236.1:c.*3680+29T>G	ENSP00000494800.1:n.*3680+29T>G
ENST00000260983.7:c.4494+29T>G	ENSP00000260983.2:n.4494+29T>G
ENST00000409111.2:c.3426+29T>G	ENSP00000386775.1:n.3426+29T>G
NM_001304840.1:c.3426+29T>G	NP_001291769.1:n.3426+29T>G
NM_020760.2:c.4494+29T>G	NP_065811.1:n.4494+29T>G
XM_006712646.2:c.4515+29T>G	XP_006712709.1:n.4515+29T>G
XM_006712648.2:c.4122+29T>G	XP_006712711.1:n.4122+29T>G
NM_001304840.2:c.3426+29T>G	NP_001291769.1:n.3426+29T>G
NM_001348768.1:c.4494+29T>G	NP_001335697.1:n.4494+29T>G
NM_020760.3:c.4494+29T>G	NP_065811.1:n.4494+29T>G
XM_006712646.3:c.4515+29T>G	XP_006712709.1:n.4515+29T>G
XM_006712648.4:c.4122+29T>G	XP_006712711.1:n.4122+29T>G
XM_024453020.1:c.4515+29T>G	XP_024308788.1:n.4515+29T>G
XM_024453021.1:c.4515+29T>G	XP_024308789.1:n.4515+29T>G
NM_001348768.2:c.4494+29T>G MANE Select	NP_001335697.1:n.4494+29T>G
NM_001304840.3:c.3426+29T>G	NP_001291769.1:n.3426+29T>G
NM_020760.4:c.4494+29T>G	NP_065811.1:n.4494+29T>G