Canonical Allele Identifier: CA1736913173
Gene: CAV2 HGNC NCBI

Linked Data

dbSNP Id: rs1382836135

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116508255A>T , CM000669.2:g.116508255A>T GRCh38
NC_000007.13:g.116148309A>T , CM000669.1:g.116148309A>T GRCh37
NC_000007.12:g.115935545A>T NCBI36
NG_029920.1:g.13655A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222693.5:c.*2134A>T MANE Select ENSP00000222693.4:n.*2134A>T
ENST00000222693.4:c.*2134A>T ENSP00000222693.4:n.*2134A>T
NM_001206747.1:c.*2134A>T NP_001193676.1:n.*2134A>T
NM_001206748.1:c.*2134A>T NP_001193677.1:n.*2134A>T
NM_001233.4:c.*2134A>T NP_001224.1:n.*2134A>T
NM_198212.2:c.*2096A>T NP_937855.1:n.*2096A>T
NM_001233.5:c.*2134A>T MANE Select NP_001224.1:n.*2134A>T
NM_001206747.2:c.*2134A>T NP_001193676.1:n.*2134A>T
NM_001206748.2:c.*2134A>T NP_001193677.1:n.*2134A>T
NM_198212.3:c.*2096A>T NP_937855.1:n.*2096A>T