Canonical Allele Identifier: CA411377912
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960855T>G (hg19) chr22:g.36564808T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564808T>G , CM000684.2:g.36564808T>G GRCh38
NC_000022.10:g.36960855T>G , CM000684.1:g.36960855T>G GRCh37
NC_000022.9:g.35290801T>G NCBI36
NG_031861.1:g.142836A>C
NG_031861.2:g.143051A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.515A>C MANE Select ENSP00000300105.6:p.Asn172Thr
ENST00000300105.6:c.515A>C ENSP00000300105.6:p.Asn172Thr
NM_006078.3:c.515A>C NP_006069.1:p.Asn172Thr
NM_006078.4:c.515A>C NP_006069.1:p.Asn172Thr
XM_017028531.2:c.257A>C XP_016884020.1:p.Asn86Thr
NM_001379051.1:c.446A>C NP_001365980.1:p.Asn149Thr
NM_006078.5:c.515A>C MANE Select NP_006069.1:p.Asn172Thr
NR_166440.1:n.1881A>C
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