Canonical Allele Identifier: CA497144530
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1406841493
gnomAD v2: 16-89245940-C-T
gnomAD v3: 16-89179532-C-T
gnomAD v4: 16-89179532-C-T
MyVariant Identifiers: chr16:g.89245940C>T (hg19) chr16:g.89179532C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179532C>T , CM000678.2:g.89179532C>T GRCh38
NC_000016.9:g.89245940C>T , CM000678.1:g.89245940C>T GRCh37
NC_000016.8:g.87773441C>T NCBI36
NG_012055.1:g.12778C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.159C>T MANE Select ENSP00000289746.2:p.Ser53=
ENST00000289746.2:c.159C>T ENSP00000289746.2:p.Ser53=
ENST00000521087.5:n.224C>T
ENST00000524089.1:n.224C>T
NM_004933.2:c.159C>T NP_004924.1:p.Ser53=
XM_011522806.1:c.159C>T XP_011521108.1:p.Ser53=
NM_004933.3:c.159C>T MANE Select NP_004924.1:p.Ser53=
Search 100 bp 5'
Search 100 bp 3'