Canonical Allele Identifier: CA514475105
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564828-G-T
MyVariant Identifiers: chr22:g.36960875G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564828G>T , CM000684.2:g.36564828G>T GRCh38
NC_000022.10:g.36960875G>T , CM000684.1:g.36960875G>T GRCh37
NC_000022.9:g.35290821G>T NCBI36
NG_031861.1:g.142816C>A
NG_031861.2:g.143031C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.495C>A MANE Select ENSP00000300105.6:p.Ser165=
ENST00000300105.6:c.495C>A ENSP00000300105.6:p.Ser165=
NM_006078.3:c.495C>A NP_006069.1:p.Ser165=
NM_006078.4:c.495C>A NP_006069.1:p.Ser165=
XM_017028531.2:c.237C>A XP_016884020.1:p.Ser79=
NM_001379051.1:c.426C>A NP_001365980.1:p.Ser142=
NM_006078.5:c.495C>A MANE Select NP_006069.1:p.Ser165=
NR_166440.1:n.1861C>A
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