Canonical Allele Identifier: CA308880117
Gene: CEACAM16-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.44719328T>G
gnomAD v3:
19:44719328 T / G
gnomAD v4:
chr19-44719328-T-G
Joint Max Group AF 0.65022628 (SAS)
Genomes Max Group AF 0.65022628 (SAS)
dbSNP:
4802234
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44719328T>G , CM000681.2:g.44719328T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
XR_935983.1:n.699-3245A>C
XR_001753954.1:n.372+5509A>C
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