Canonical Allele Identifier: CA885343940
Gene: CELSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1229953502
gnomAD v4: 1-109263940-G-A
MyVariant Identifiers: chr1:g.109806562G>A (hg19) chr1:g.109263940G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109263940G>A , CM000663.2:g.109263940G>A GRCh38
NC_000001.10:g.109806562G>A , CM000663.1:g.109806562G>A GRCh37
NC_000001.9:g.109608085G>A NCBI36
NG_052669.1:g.19236G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-138G>A MANE Select ENSP00000271332.3:n.5002-138G>A
ENST00000271332.3:c.5002-138G>A ENSP00000271332.3:n.5002-138G>A
NM_001408.2:c.5002-138G>A NP_001399.1:n.5002-138G>A
XM_005270580.3:c.5002-138G>A XP_005270637.1:n.5002-138G>A
NM_001408.3:c.5002-138G>A MANE Select NP_001399.1:n.5002-138G>A
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