Canonical Allele Identifier: CA2646919013
Gene: CELSR2 HGNC NCBI

Linked Data

gnomAD v4: 1-109274576-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109274576C>A , CM000663.2:g.109274576C>A GRCh38
NC_000001.10:g.109817198C>A , CM000663.1:g.109817198C>A GRCh37
NC_000001.9:g.109618721C>A NCBI36
NG_052669.1:g.29872C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000271332.4:c.*527C>A MANE Select ENSP00000271332.3:n.*527C>A
ENST00000271332.3:c.*527C>A ENSP00000271332.3:n.*527C>A
ENST00000498157.1:n.2649C>A
NM_001408.2:c.*527C>A NP_001399.1:n.*527C>A
XM_005270580.3:c.*394C>A XP_005270637.1:n.*394C>A
NM_001408.3:c.*527C>A MANE Select NP_001399.1:n.*527C>A
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