Canonical Allele Identifier: CA497144543
Gene: CDH15 HGNC NCBI

Linked Data

gnomAD v4: 16-89179559-C-G
MyVariant Identifiers: chr16:g.89245967C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179559C>G , CM000678.2:g.89179559C>G GRCh38
NC_000016.9:g.89245967C>G , CM000678.1:g.89245967C>G GRCh37
NC_000016.8:g.87773468C>G NCBI36
NG_012055.1:g.12805C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000289746.3:c.186C>G MANE Select ENSP00000289746.2:p.Pro62=
ENST00000289746.2:c.186C>G ENSP00000289746.2:p.Pro62=
ENST00000521087.5:n.251C>G
ENST00000524089.1:n.251C>G
NM_004933.2:c.186C>G NP_004924.1:p.Pro62=
XM_011522806.1:c.186C>G XP_011521108.1:p.Pro62=
NM_004933.3:c.186C>G MANE Select NP_004924.1:p.Pro62=
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