Canonical Allele Identifier: CA411378489
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960921A>C (hg19) chr22:g.36564874A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564874A>C , CM000684.2:g.36564874A>C GRCh38
NC_000022.10:g.36960921A>C , CM000684.1:g.36960921A>C GRCh37
NC_000022.9:g.35290867A>C NCBI36
NG_031861.1:g.142770T>G
NG_031861.2:g.142985T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.449T>G MANE Select ENSP00000300105.6:p.Ile150Ser
ENST00000300105.6:c.449T>G ENSP00000300105.6:p.Ile150Ser
NM_006078.3:c.449T>G NP_006069.1:p.Ile150Ser
NM_006078.4:c.449T>G NP_006069.1:p.Ile150Ser
XM_017028531.2:c.191T>G XP_016884020.1:p.Ile64Ser
NM_001379051.1:c.380T>G NP_001365980.1:p.Ile127Ser
NM_006078.5:c.449T>G MANE Select NP_006069.1:p.Ile150Ser
NR_166440.1:n.1815T>G
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