Canonical Allele Identifier: CA323997826
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs111933816
MyVariant Identifiers: chr22:g.36960867T>G (hg19) chr22:g.36564820T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564820T>G , CM000684.2:g.36564820T>G GRCh38
NC_000022.10:g.36960867T>G , CM000684.1:g.36960867T>G GRCh37
NC_000022.9:g.35290813T>G NCBI36
NG_031861.1:g.142824A>C
NG_031861.2:g.143039A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.503A>C MANE Select ENSP00000300105.6:p.Asp168Ala
ENST00000300105.6:c.503A>C ENSP00000300105.6:p.Asp168Ala
NM_006078.3:c.503A>C NP_006069.1:p.Asp168Ala
NM_006078.4:c.503A>C NP_006069.1:p.Asp168Ala
XM_017028531.2:c.245A>C XP_016884020.1:p.Asp82Ala
NM_001379051.1:c.434A>C NP_001365980.1:p.Asp145Ala
NM_006078.5:c.503A>C MANE Select NP_006069.1:p.Asp168Ala
NR_166440.1:n.1869A>C
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