Canonical Allele Identifier: CA2342626759
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs2069339614
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977930C>T , CM000681.2:g.53977930C>T GRCh38
NC_000019.9:g.54481184C>T , CM000681.1:g.54481184C>T GRCh37
NC_000019.8:g.59172996C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270458.4:c.284-216C>T MANE Select ENSP00000270458.3:n.284-216C>T
ENST00000270458.2:c.284-216C>T ENSP00000270458.2:n.284-216C>T
NM_031895.5:c.284-216C>T NP_114101.4:n.284-216C>T
NM_031895.6:c.284-216C>T MANE Select NP_114101.4:n.284-216C>T
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