Canonical Allele Identifier: CA497144547
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs764989466
gnomAD v2: 16-89245973-C-G
gnomAD v3: 16-89179565-C-G
gnomAD v4: 16-89179565-C-G
MyVariant Identifiers: chr16:g.89245973C>G (hg19) chr16:g.89179565C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179565C>G , CM000678.2:g.89179565C>G GRCh38
NC_000016.9:g.89245973C>G , CM000678.1:g.89245973C>G GRCh37
NC_000016.8:g.87773474C>G NCBI36
NG_012055.1:g.12811C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.192C>G MANE Select ENSP00000289746.2:p.Pro64=
ENST00000289746.2:c.192C>G ENSP00000289746.2:p.Pro64=
ENST00000521087.5:n.257C>G
ENST00000524089.1:n.257C>G
NM_004933.2:c.192C>G NP_004924.1:p.Pro64=
XM_011522806.1:c.192C>G XP_011521108.1:p.Pro64=
NM_004933.3:c.192C>G MANE Select NP_004924.1:p.Pro64=
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