Canonical Allele Identifier: CA8238724
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs772607179
ExAC: 16:89246034 T / C
gnomAD v2: 16-89246034-T-C
gnomAD v4: 16-89179626-T-C
MyVariant Identifiers: chr16:g.89246034T>C (hg19) chr16:g.89179626T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179626T>C , CM000678.2:g.89179626T>C GRCh38
NC_000016.9:g.89246034T>C , CM000678.1:g.89246034T>C GRCh37
NC_000016.8:g.87773535T>C NCBI36
NG_012055.1:g.12872T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+52T>C MANE Select ENSP00000289746.2:n.201+52T>C
ENST00000289746.2:c.201+52T>C ENSP00000289746.2:n.201+52T>C
ENST00000521087.5:n.266+52T>C
ENST00000524089.1:n.266+52T>C
NM_004933.2:c.201+52T>C NP_004924.1:n.201+52T>C
XM_011522806.1:c.201+52T>C XP_011521108.1:n.201+52T>C
NM_004933.3:c.201+52T>C MANE Select NP_004924.1:n.201+52T>C
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