Canonical Allele Identifier: CA2646919067
Gene: CELSR2 HGNC NCBI

Linked Data

gnomAD v4: 1-109274585-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109274585A>T , CM000663.2:g.109274585A>T GRCh38
NC_000001.10:g.109817207A>T , CM000663.1:g.109817207A>T GRCh37
NC_000001.9:g.109618730A>T NCBI36
NG_052669.1:g.29881A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000271332.4:c.*536A>T MANE Select ENSP00000271332.3:n.*536A>T
ENST00000271332.3:c.*536A>T ENSP00000271332.3:n.*536A>T
ENST00000498157.1:n.2658A>T
NM_001408.2:c.*536A>T NP_001399.1:n.*536A>T
XM_005270580.3:c.*403A>T XP_005270637.1:n.*403A>T
NM_001408.3:c.*536A>T MANE Select NP_001399.1:n.*536A>T
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