Canonical Allele Identifier: CA883512808
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs1190187965
MyVariant Identifiers: chr19:g.54481085C>G (hg19) chr19:g.53977831C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977831C>G , CM000681.2:g.53977831C>G GRCh38
NC_000019.9:g.54481085C>G , CM000681.1:g.54481085C>G GRCh37
NC_000019.8:g.59172897C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270458.4:c.284-315C>G MANE Select ENSP00000270458.3:n.284-315C>G
ENST00000270458.2:c.284-315C>G ENSP00000270458.2:n.284-315C>G
NM_031895.5:c.284-315C>G NP_114101.4:n.284-315C>G
NM_031895.6:c.284-315C>G MANE Select NP_114101.4:n.284-315C>G
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