Canonical Allele Identifier: CA763326567
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1173031127
gnomAD v3: 2-201287996-A-G
gnomAD v4: 2-201287996-A-G
MyVariant Identifiers: chr2:g.202152719A>G (hg19) chr2:g.201287996A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287996A>G , CM000664.2:g.201287996A>G GRCh38
NC_000002.11:g.202152719A>G , CM000664.1:g.202152719A>G GRCh37
NC_000002.10:g.201860964A>G NCBI36
NG_007497.1:g.59539A>G , LRG_34:g.59539A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2679A>G ENSP00000512371.1:n.1259+2679A>G
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