Canonical Allele Identifier: CA411377953
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960858T>G (hg19) chr22:g.36564811T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564811T>G , CM000684.2:g.36564811T>G GRCh38
NC_000022.10:g.36960858T>G , CM000684.1:g.36960858T>G GRCh37
NC_000022.9:g.35290804T>G NCBI36
NG_031861.1:g.142833A>C
NG_031861.2:g.143048A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.512A>C MANE Select ENSP00000300105.6:p.Lys171Thr
ENST00000300105.6:c.512A>C ENSP00000300105.6:p.Lys171Thr
NM_006078.3:c.512A>C NP_006069.1:p.Lys171Thr
NM_006078.4:c.512A>C NP_006069.1:p.Lys171Thr
XM_017028531.2:c.254A>C XP_016884020.1:p.Lys85Thr
NM_001379051.1:c.443A>C NP_001365980.1:p.Lys148Thr
NM_006078.5:c.512A>C MANE Select NP_006069.1:p.Lys171Thr
NR_166440.1:n.1878A>C
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