Canonical Allele Identifier: CA1736913121
Gene: CAV2 HGNC NCBI

Linked Data

dbSNP Id: rs1793287078

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116508178A>G , CM000669.2:g.116508178A>G GRCh38
NC_000007.13:g.116148232A>G , CM000669.1:g.116148232A>G GRCh37
NC_000007.12:g.115935468A>G NCBI36
NG_029920.1:g.13578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222693.5:c.*2057A>G MANE Select ENSP00000222693.4:n.*2057A>G
ENST00000222693.4:c.*2057A>G ENSP00000222693.4:n.*2057A>G
NM_001206747.1:c.*2057A>G NP_001193676.1:n.*2057A>G
NM_001206748.1:c.*2057A>G NP_001193677.1:n.*2057A>G
NM_001233.4:c.*2057A>G NP_001224.1:n.*2057A>G
NM_198212.2:c.*2019A>G NP_937855.1:n.*2019A>G
NM_001233.5:c.*2057A>G MANE Select NP_001224.1:n.*2057A>G
NM_001206747.2:c.*2057A>G NP_001193676.1:n.*2057A>G
NM_001206748.2:c.*2057A>G NP_001193677.1:n.*2057A>G
NM_198212.3:c.*2019A>G NP_937855.1:n.*2019A>G