Canonical Allele Identifier: CA633855851
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs1394391770
gnomAD v2: 19-54481161-T-TA
gnomAD v3: 19-53977907-T-TA
gnomAD v4: 19-53977907-T-TA
MyVariant Identifiers: chr19:g.54481161_54481162insA (hg19) chr19:g.53977907_53977908insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977908dup , CM000681.2:g.53977908dup GRCh38
NC_000019.9:g.54481162dup , CM000681.1:g.54481162dup GRCh37
NC_000019.8:g.59172974dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-238dup MANE Select ENSP00000270458.3:n.284-238dup
ENST00000270458.2:c.284-238dup ENSP00000270458.2:n.284-238dup
NM_031895.5:c.284-238dup NP_114101.4:n.284-238dup
NM_031895.6:c.284-238dup MANE Select NP_114101.4:n.284-238dup
Search 100 bp 5'
Search 100 bp 3'